ActivMed Practices and Research, Inc. has been conducting sophisticated clinical research trials on behalf of the world's leading pharmaceutical biotechnology and medical device companies for more than 20 years. The company has been recognized for patient care, patient recruitment and a high standard of protocol delivery. Our expertise and experience make us the first choice for clinical trials in Northern Massachusetts and Southern New Hampshire.

Advanced Clinical Research, the first community based clinical research centers in both Utah and Idaho, was founded in 1984. ACR Utah's Research Center has extensive experience in a variety of therapeutic areas, having managed over 700 clinical studies and enrolling more than 9,000 patients. ACR Idaho's experience base is also substantial, having been established in 1991. ACR's success is a result of our longstanding affiliations with some of the largest independent group practices in Utah and Idaho, dedicated physician/investigators, and a committed ACR staff.

For more than 25 years, Advanced Clinical Research Institute has been dedicated to assisting pharmaceutical companies find new cures to help patients better manage their healthcare. We share in the commitment and dedication to providing cutting edge therapy that can assist in managing patients' chronic medical conditions today and for a lifetime. In the clinical trials area, ACRI offers investigational therapies for indications such as Migraines, Insomnia, Chronic Pain, Osteoporosis, Hormone Replacement Therapy, Diabetes and much more. We offer new and existing therapies that manage conditions where other medical therapies may have failed. Each and every patient at ACRI receives the highest quality medical care. We notify the patient's primary care physician of enrollment and ongoing status and provide a full report at the conclusion of each study.

Created in 1997, the American Stroke Association is dedicated to prevention, diagnosis and treatment to save lives from stroke - America's No. 4 killer and a leading cause of serious disability. We fund scientific research, help people better understand and avoid stroke, encourage government support, guide healthcare professionals and provide information to enhance the quality of life for stroke survivors. Our mission is to build healthier lives, free of cardiovascular diseases and stroke. That single purpose drives all we do. The need for our work is beyond question.

The American Academy of CME, Inc., is an independent, nonprofit, accredited provider of continuing medical education for physicians, pharmacists, nurses and dieticians. The Academy’s mission is to enhance the quality and effectiveness of patient care through innovative delivery and support of continuing professional development programs for health care professionals. The Academy partners with medical education and communication companies and other organizations to provide certified continuing education for health care professionals.

The American Art Therapy Association, Inc. (Association) is an organization of professionals dedicated to the belief that making art is healing and life enhancing. Its mission is to serve its members and the general public by providing standards of professional competence, and developing and promoting knowledge in, and of, the field of art therapy.

Art therapy is a mental health profession that uses the creative process of art making to improve and enhance the physical, mental and emotional well-being of individuals of all ages. Research in the field confirms that the creative process involved in artistic self-expression helps people to resolve conflicts and problems, develop interpersonal skills, manage behavior, reduce stress, increase self-esteem and self-awareness, and achieve insight.

ASKA Research, a Division of Valerie Willetts & Associates Inc., was founded in 1995 ASKA Research provides a full range of multi-centre clinical trial management and monitoring services from project conception to marketing approval.

La Asociación Mexicana de Enfermedad Vascular Cerebral, A.C. "AMEVASC" inició sus actividades científicas el 30 de Octubre de 2000. El objetivo principal de AMEVASC es sin duda el estudio, investigación y educación médica continua de la enfermedad vascular cerebral "EVC", la cual representa la segunda causa de muerte y primera de discapacidad a nivel mundial. Siempre a la vanguardia, y conscientes que la tecnología se ha convertido en una herramienta indispensable de las ciencias médicas, AMEVASC incurciona en el área de la informática médica, poniendo a su servicio AMEVASC On-line! el nuevo portal de Neurociencias Vasculares.

Aspen Clinical Research is a leading clinical research Phase I-IV research center located in Orem Utah. We diversify our therapeutic areas by employing highly skilled and experienced physicians in a variety of specialties. Aspen Research's specialties in medicine range from Psychiatric medicine, Endocrinology, Acute and Chronic Pain Management, Oncology, Cardiovascular medicine, Internal medicine, Family practice, Plastic surgery, Podiatry, Infectious diseases, Pulmonology, Pediatric Medicine, Physiatry, Emergency Medicine, and Oral Maxillofacial surgery.

The Atlantic Center for Research serves as a central point of contact for sponsors and investigators of clinical trials who are affiliated with our hospitals, as well as attending physicians interested in conducting a clinical trial and physicians looking to refer a patient to a research study. We facilitate and coordinate all clinical research activities to expedite study initiation and to ensure strict compliance with the highest standards of research conduct.

The Atlantic Center for Research offers: Centralized clinical trial management, Extensive experience in pharmaceutical and medical device trials, Diverse inpatient and outpatient populations, Expert oversight of clinical trial conduct, Professional, experienced clinical research coordinators, Physician investigators in all specialties, Centralized IRB review, Subject recruitment and screening, Strict compliance with FDA and good clinical practice standards, Complete financial and administrative management, Prompt review and execution of contracts, Dedicated, experienced research pharmacists

At Beyer Research we have experienced clinical research coordinators, skilled nurse practitioners and knowledgeable administrators who work together to conduct clinical research trials.

In a clinical trial, new treatments, drugs, diagnostic tests, procedures or other therapies are tested on human participants to see if they are safe and effective. We conduct clinical trials in multiple therapeutic areas. Our staff is dedicated to maintaining the integrity of the research, safety, and protection of our patients. Beyer Research is affiliated with Women's Health Care Specialists P.C., a full-service women's health facility in business since 1984.

BioQ Solutions is dedicated to helping clients achieve and maintain their compliance with GCP, GMP, GLP, and GTP regulatory requirements and industry standards through efficient and effective quality systems. Our services include clinical trial management and monitoring; quality system design and implementation; FDA inspection and response support; information systems assessment and implementation; audits (internal, vendor, sponsor, investigator); process and procedure development or design; and training development and delivery.

The Biomedical Research Alliance of New York (BRANY) offers several educational programs through the BRANY Institute for Research Education. Courses are offered at the BRANY offices in Lake Success, NY. We will also present any BRANY course at your institution or organization anywhere in the world. Our instructors include experts in the fields of research compliance and IRB standards. Who should take these classes? These classes are a must for any clinical research professional including principal investigators, research coordinators, research pharmacists, regulatory coordinators, and data managers who need to be familiar with the federal regulations, ethical guidelines, and processes involved in the conduct of human subject research.

Cato Research is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them.

CDISC is a global, open, multidisciplinary, non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. The CDISC mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare. CDISC standards are vendor-neutral, platform-independent and freely available via the CDISC website.

The CDISC Vision is to Inform Patient Care & Safety Through Higher Quality Medical Research.

Clearview Medical Research is a high caliber, clinical research provider that conducts Phase II-IV studies. We are located in Los Angeles County, in the cities of Glendale and Santa Clarita. At CMR, we are dedicated to providing customized services capable of quickly responding to the changing needs of the Sponsor, CRO, and Study Volunteer. Maintaining strong working relationships through good communication among members of the research team is priority during and after the study. Our staff is a mix of diverse educational backgrounds with experience in clinical research coordination, project management, patient recruitment, information technology, group facilitation, and public health education. The CMR Principle Investigator Marina Gold M.D. has over 40 years of medical experience and a passion for research. Above all, our goal is to provide a safe, comfortable, and beneficial experience for our volunteers.

Clinsys Clinical Research, Inc. is a full-service clinical research organization -CRO- that provides pharmaceutical, biotechnology and medical device companies with a broad range of clinical research services in support of Phase I-IV drug and device development, including project management, clinical monitoring, scientific and medical support, investigator and patient recruitment, site management, biostatistics, data management, drug safety, quality assurance, regulatory affairs, and medical writing.

ClinTrial Networks consists of a group of independently owned investigator sites located throughout the United States, however we are not an SMO. Sites complete their own CDA's Feasibility Questionnaires and regulatory documents. Each site has extensive research experience and conduct studies across a broad range of therapeutic areas. Each site has a dedicated research staff consisting of highly trained investigators and study coordinators, uses central IRBs with start-up regulatory document turnaround time within 5 days, and is in full compliance with FDA, GCP, ICH, and IRB guidelines.

CNS Ratings LLC provides rater training and protocol consultation on Rating Scales for US and international studies in pediatric, adult and geriatric CNS clinical trials. We’ve been doing this for 20 years. The company is headed by Dr. Paul Michael Ramirez who is a Doctoral Program Professor of Neuropsychology / Neuroscience and Psychopathology in Clinical Psychology at Long Island University’s Brooklyn, New York Campus. He also teaches Psychopharmacology within the Pharmaceutical Sciences Graduate Program of the College of Pharmacy and Health Sciences at LIU.

CNS Ratings LLC provides rater training and protocol consultation on Rating Scales for US and international studies in pediatric, adult and geriatric CNS clinical trials. We’ve been doing this for 20 years. The company is headed by Dr. Paul Michael Ramirez who is a Doctoral Program Professor of Neuropsychology / Neuroscience and Psychopathology in Clinical Psychology at Long Island University’s Brooklyn, New York Campus. He also teaches Psychopharmacology within the Pharmaceutical Sciences Graduate Program of the College of Pharmacy and Health Sciences at LIU.

CNS Research, Inc. was founded in 1997 by Patricia J. Epple, RN, BS, CCRC as a multi-site PPPN, (Private Practice Physician's Network). Our goal is to provide the best possible patient care by offering clinical research opportunities with medications not available to the general public. Our Network is comprised of leading neurologists in Southern New England. We focus on research phases II, III, & IV. Therapeutic specialties are Alzheimer's Disease, Diabetic Neuropathic Pain, Stroke, Epilepsy, Migraine Headaches, Multiple Sclerosis, Vascular Dementia. Having worked with pharmaceutical companies for over a decade, we have come to understand all aspects of the research process. With this broad experience, we have added other research services, such as monitoring for sites outside our network.

The College of Psychiatric and Neurologic Pharmacists (CPNP) was founded on March 24, 1998 when the network of pharmacists formerly known as the Conference of Psychiatric and Neurologic Pharmacists became a professional society. The formation of CPNP was the culmination of efforts of many pharmacists practicing in the psychiatry and neurology specialties over the past 30 years. CPNP has continued to evolve and grow and has increased membership to over 1,000 individuals.

ConnecTrial is a company that finds study opportunities for clinical research sites. Site Managers can run into various difficulties when attempting to develop business for their sites: 1.) They are too busy with operational activities. 2.) They may not have enough contacts in the industry. 3.) They cannot afford their own dedicated business development staff. ConnecTrial addresses these issues by providing sites with immediate business development support. We contact CROs and Sponsors on behalf of sites to find study opportunities sites otherwise might have missed - at a surprisingly low price.

We are a dedicated medical research facility with locations in Beaumont and Bryan/College Station, Texas, which began operations in April 1999 and April 2002, respectively. The sole focus of our organization is to bring clinical research studies to the local market, where our company collaborates with local physicians and community health organizations to conduct medical research studies, otherwise known as “clinical research”. All clinical research studies at DiscoveResearch are under the medical supervision of local physicians, conducted in strict compliance with federal regulations established and enforced by the US Food and Drug Administration.

DM Clinical Research (DM) is a network of investigator sites based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with several qualified physicians with a diverse range of specialties and have conducted a wide variety of studies with successful enrollment targets. Our team of coordinators are highly educated and trained in medicine and research and include medical graduates.

DSP executives and support staff come directly from the pharmaceutical and biotech industries, enabling us to better understand your needs and view studies from your perspective. We are skilled at identifying and resolving potential study issues early on and strategically allocating resources to ensure project completion on time and on-budget. We always have Plan B in place when studies do not go as anticipated. At DSP, we have developed proven internal SOPs and QA metrics to ensure that quality systems are in place and rigorously followed during every client's clinical study. In the past several years we have managed and/or monitored more than 50 Phase I - IV clinical trials in various therapeutic areas and have filed 15 New Drug Applications.

DWD Associates is a group of experienced clinical research professionals. We have backgrounds in both early development and late phase in both sponsor and investigator organizations. We include ex–FDA investigators with both sponsor and site inspection experience. We are seasoned professionals who bring our experiences to your organization. Donna W. Dorozinsky founded DWD & Associates in 2005. Prior to this she was involved in the conduct of clinical trials for over 15 years, with a primary focus on industry based studies. She has significant clinical experiences in Phase I operations. Donna is president–elect of the Association of Clinical Pharmacology Units and has served as adjunct faculty at Drexel University College of Nursing and College of Medicine.

Echo Earth Media is the industry’s “go to” powerhouse for award-winning creative and multimedia talent. As a national multimedia communications firm we work with diverse industry leaders, world class brands and emerging companies to help them create, redefine and bring to market innovative products, services and experiences. And, we can do the same for you. Our multidisciplinary process reveals the depth of your brand, product and the people you touch, leading to valuable consumer and market insights for lasting solutions, and with our team of thought leaders, designers, technologists and strategists, we can deliver fully convergent experiences across multiple technologies, platforms and media.

ECLINSO was founded 1995 in Basel, Switzerland initially providing consultancy services to the pharmaceutical and telecommunication industry. Following significant growth in the pharmaceutical sector we decided in 2002 to fully focus on delivering Managed IT services and Support services to the pharmaceutical industry. Our expansion led to a number of highly successful integrated solutions and services being developed for Life Sciences Clients. Consequently in 2004 we secured our first large global account, enabling us to expand globally.

In 2008 we continued to expand our portfolio to include Electronic Data Capture, Document Management and Regulatory solutions. Today, through trialforce we offer a comprehensive Cloud based Software as a Service (SaaS) platform, providing infrastructure and services, that have been purposely designed to keep pace with the increasing complexity of Clinical discovery. It offers unparalleled flexibility and adaptability to both Sponsors and Clinical research organizations (CRO's). Using a SaaS subscription model we deliver an innovative, affordable, scalable and easy-to-use platform that enables sponsors and CRO's of all sizes to rapidly deploy an integrated eClinical suite. Key to our continued success has been our superior service delivery in Project Management, Study Design, Training and client Support.

Exceptional Education Outreach (EEO) is a public, non-profit special education and literacy project operating in the Bahamian Family Islands. EEO strives to provide special education and literacy outreach programs to students and their communities in Eleuthera and Harbour Island. We do this through direct service in schools, training programs for teachers and parents, and professional medical assistance to underserved students.

Endeavor Clinical Trials, PA is a privately owned, multi-therapeutic, dedicated research center set up to conduct phase II-IV trials. Located in the Medical Center of San Antonio, Texas, we are approximately 20 minutes from the San Antonio International Airport and within minutes of several hotels. Endeavor Clinical Trials is owned and operated by Richard A. Pollak, DPM, MS. Dr. Pollak has over 15 years experience in conducting clinical trials as a principal investigator. Dr. Pollak, along with numerous physicians located throughout the Medical Center, act as the investigators for the studies which we conduct. Endeavor Clinical Trials staff consists of experienced Clinical Research Coordinators and Clinical Research Assistants. Our staff prides itself in delivering accurate, viable data to our clients while maintaining quality patient care. Every subject visit conducted is QC'd to ensure quality data is delivered. We value teamwork, integrity, productivity, accountability and professionalism. Our Coordinators are available to work closely with the CRAs during their visit to streamline the data collection process and ensure our clients meet their goals in a timely manner.

Florida Premier Research Institute, and Florida Pulmonary Research Institute are State-of-the-Art, Multi-Specialty facilities conducting Phase I-IV clinical trials in the Orlando, Florida, metropolitan area. Our Principal Investigator, Dr. Faisal A. Fakih and staff are fully committed to finding new medical treatments to improve the millions of lives affected by a serious illness. Participants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.

GPC provides consultancy & services in the following areas: Clinical Research, Clinical Operations, QA & Compliance Auditors Network, Cognitive Drug Tests & Psychiatric and Clinical Assessments, Drug Safety & Pharmacovigilance and Business Initiatives

GPC provides consultancy & services in the following areas: Clinical Research, Clinical Operations, QA & Compliance Auditors Network, Cognitive Drug Tests & Psychiatric and Clinical Assessments, Drug Safety & Pharmacovigilance & Business Initiatives.

Goodwyn IRB provides a wide range of services for the review and oversight of clinical studies. Our customers are pharmaceutical and device manufacturers (sponsors) and the contract research and site management organizations that serve them. We also serve institution and physician-sponsors. Here's our list of services. Or, perhaps we can design a custom program to fit your unique requirements. Initial and ongoing review of clinical research protocols and investigative sites (including the informed consent process and study-related materials) - On-line IRB study document submission tracking - delivery of IRB research review documentation within 48-hours of the review - Good Clinical Practice (GCP) audits and training - On-site evaluation of the informed consent process - Informed consent writing, templates & translations - Statistical support for de-identification of protected health information.

A Site Management Organization (SMO) named HarborWay Clinical LLC, has been established in Mississippi to perform clinical trials in private practice clinics. The founder of this business, Dr. John Piletz, has been a full Professor of NeuroPsychiatry at various medical schools beginning at the University of Mississippi Medical Center in 1998. His formal postdoctoral training includes Biochemistry, Molecular Genetics, Psychopharmacology, Cardiovascular Physiology, and Psychiatry. Dr. Piletz has published more than 100 original research articles and holds several drug patents. The impetus for starting the business was a realization that academia has become non-competitive with a "flat earth" across which most phases of clinical trials are now run (with the possible exception of Phase I clinical trials). Dr. Piletz therefore has been forming a local SMO network within the private practice clinics of Mississippi. The state of Mississippi offers many advantages for conducting clinical trials which include a large patient to doctor ratio, an abundance of private practices, and needy patients. In addition, a large minority population exists here for which health disparities should not be overlooked when clinical trials become available.

We provide services in Clinical trials which are studies that evaluate the effectiveness and safety of new medications or devices. The Food and Drug Administration (FDA) requires vigorous efforts by the sponsor company (i.e. pharmaceutical companies, device manufacturers) and investigators, such as the physicians at Idaho Urologic Institute, to provide accurate and quality data, while practicing under the guidelines of Good Clinical Practice (GCP), to determine if an investigational medication or device should be approved for marketing. The advancement of medicine is dependent upon clinical trials and the participation of patients who live each day with the diseases and illnesses that plague our country.

INC Research has a deep-rooted history of therapeutic expertise and technological innovation. Founded more than two decades ago as an academic research organization focused on CNS research, we've translated that expertise into a global organization with the added specialties of infectious diseases, oncology and pediatrics, as well as full data services capabilities. Throughout the 1980s, the University of Virginia at Charlottesville was the site of several pivotal head injury and cerebrovascular studies. In 1985, those programs were consolidated into the Brain Injury Research Program (BIRP), which forms the basis of INC Research. Six years later, the Neuroclinical Trials Center (NTC) was chartered, and the staff of the BIRP became part of the NTC. From 1991 through 1998, NTC staff participated in more than 40 global CNS clinical trials involving 20,000 patients in North America, Europe and Australasia. In 1996, NTC became one of the first adopters of Oracle Clinical™. Along with strategic partners in the industry, NTC played a major role in the co-development of Oracle's data clarification forms subsystem, as well as a CRF tracking module.

Founded in 1999, IntegReview applies ethics and integrity to research while accelerating the IRB process with technology, offers multiple weekly meetings, two-day turnaround, expert reviewers, flexible personal service, knowledgeable/available staff.

Investigator Support Services (ISS) provides clinical trial support tailored to the specific needs of our life sciences clients and research site partners. Through our breadth of services and personal attention to each trial, we support drug and device development from site selection through patient compliance. ISS reduces the time and money associated with site selection through direct access to 1400 vetted phase I-IV research sites in North America and India. At no cost, investigators are pre-qualified and submitted for clinical trials based on individual study needs. We provide business development services to our research site partners through access to a steady stream of new clinical trial opportunities in all phases and therapeutic areas. To supplement internally identified projects, investigators may consider hundreds of clinical trials annually, with new opportunities matched to site capabilities and research expertise. ISS delivers patient recruitment and compliance solutions through our global healthcare contact center services and strategic alliances with patient recruitment firms. With more than a decade of experience supporting drug development, we know how to match the right resources to the complex needs of sponsors and CROs.

Kestrel understands that clinical research and development are high-risk and constantly evolving. Organizations and regulators increasingly demand high quality data that meet industry standards. With over 25 years of industry and academic experience, and leadership roles in CDISC and other standards and quality activities, Kestrel provides cutting edge education that helps you design and manage your data to meet these challenges. We offer on demand courses on Training Campus as well as custom on-site classes, which are cost-effective solutions to today's training requirements. Kestrel is a CDISC Registered Solution Provider and an Official Trainer for CDASH.

We specialize in complex linguistic translation, localization and interpreting projects with unique technical and logistical requirements. Established in 1993, Language Connections is headquartered in Boston, MA with satellite offices in major world centers. In order to serve our clients better, we employ a network of experts – translators, editors and interpreters worldwide – to assure competent, timely and cost-effective support. Our linguists specialize in energy, engineering, high tech and advanced sciences, pharmaceutical, medical, biotech, legal, marketing and business translations. Their work is coordinated by our experienced and efficient Account and Project Managers. We use the latest translation industry software tools to guarantee consistency, savings and top quality services. We translate web sites, scientific articles, patents, clinical documents and other culturally sensitive materials.

Formerly SIPLAS RO, Latam Clinical Trials is a full service contract research organization (CRO), offering nanotechnology, biopharmaceutical and medical device companies comprehensive monitoring and management services for conducting Phase II-IV clinical trials in Latin America.

Founded in 2000, Lernia Training Solutions LLC specializes in the creation, delivery and management of training for the pharmaceutical industry. We design customized training programs for companies of all sizes in order to help them meet regulatory requirements and have their employees equipped with working knowledge of the subject matter at hand. Our customized training programs are based on an alignment with your company's business processes. In using a proven methodology we enable your company to gain efficiencies by eliminating the need for training twice - once on the core system application or regulatory documents and again with your company's specific process details.

Mission: MAGI’s mission is to standardize best practices for clinical research operations, business and regulatory compliance. "MAGI" is pronounced with "G" as in Georgia and "I" as in Ireland. "MAGI" originally stood for Model Agreement Group Initiative, but our scope is now much broader than clinical trial agreements, so the acronym has no meaning. Suggestions are invited.

Since 1997 Maine Labpack, Inc. has been meeting all requirements for the safe and proper disposal of Hazardous, Universal, Bio-Hazardous and Non-Hazardous wastes and materials. MLI is dedicated to the packing of waste for transport and disposal to fully regulated and authorized disposal facilities and providing emergency response services.

MAPS Applied Research Center (MARC) is a privately owned clinical investigative site that conducts multi-therapeutic outpatient phase I-IV clinical trials. MARC is committed to deliver innovative, state of the art medical research to our community while assisting pharmaceutical and device companies in bringing new products to market. Since 1999, MARC has conducted over 100 trials across a wide range of therapeutic areas including: Pain Management (Acute, Chronic and Interventional), Neurology, Gastrointestinal, Muscular/Skeletal, Dermatology, Mental Health, Cardiovascular, Endocrinology/Metabolic, Sleep Medicine, Bone and Joint Disease, Infectious Disease, Autoimmune Disease, Women’s Health, Nutraceuticals and Pharmacokinetics.

Maximum Advantage is an organizational development company helping companies to hire, develop, and retain superstar individuals and employees. Our emphasis is on using psychology for effective communication to motivate, persuade, resolve conflict, and build strong teams.

When you work with Medicor Research you get the advantages of working with the physician’s office as well as an SMO. Over 40 physicians and specialists functioning as Principal Investigators, Sub-Investigators, Co-Investigators and thought leaders entrust Medicor to coordinate their clinical trials in the Sudbury region. All of our physicians are trained in GCP-ICH upon joining Medicor; they understand their roles and obligations and how our support teams fit into the execution of clinical trials from the feasibility process straight through to study archiving. Our physicians work in groups which has created a huge referral network guaranteeing targets are consistently met or exceeded quickly.

We offer support services for a number of customer types in the clinical trials, research, and drug development fields: Clinical Trials Site, Contract Research Organization, Pharmaceutical Sponsor, Academic Institution, Independent Researcher/Developer.

The National Institute of Neurological Disorders and Stroke (NINDS) conducts and supports research on brain and nervous system disorders. Created by the U.S. Congress in 1950, NINDS is one of the more than two dozen research institutes and centers that comprise the National Institutes of Health (NIH). The NIH, located in Bethesda, Maryland, is an agency of the Public Health Service within the U.S. Department of Health and Human Services. NINDS has occupied a central position in the world of neuroscience for 50 years.

NIH is the steward of medical and behavioral research for the Nation. Its mission is science in pursuit of fundamental knowledge about the nature and behavior of living systems and the application of that knowledge to extend healthy life and reduce the burdens of illness and disability. ...the NIH provides leadership and direction to programs designed to improve the health of the Nation by conducting and supporting research...

At National Stroke Association we are committed to providing you with the information and tools you need to prevent and treat stroke in your patients — no matter where you work along the continuum of stroke care.

We provide access to most promising new medical and psychiatric treatment options. We are committed to pioneering new therapies to treat medical and psychiatric illnesses. Moreover, we are just as passionate about creating a supportive, caring environment for our patients and their families. We conduct leading-edge research in key areas, giving rise to new hope for tomorrow. Patient volunteers are engaged from the greater Akron and Canton, Ohio metropolitan area. The combined population of surrounding Stark, Summit, Mahoning, Portage, and Harrison counties exceeds 1.4 million people.

The National Institute of Neurological Disorders and Stroke (NINDS) Clinical Research Collaboration (CRC) is a new opportunity for physicians and patients who want to learn about or participate in research studies of neurological diseases.

OCR is an independent research site located in Salt Lake City, UT. Partnering with pharmaceutical companies, OCR studies the safety and efficacy of investigational medication in the population at the final stages of the FDA approval process. OCR provides comprehensive facilities for the conduct of clinical research in a comfortable, yet professional environment. At Optimum Clinical Research, we pride ourselves on putting our participants first. Informed consent is our priority. Before you enter into a clinical trail here at Optimal Clinical Research, you will be educated at length on the key facts concerning your specific type of research. This education gives you the power to decide whether or not the study is going to be right for you.

At OptumHealth Education, we integrate medical expertise and adult learning principles with dynamic technology to deliver compelling CME programming to health care professionals in a variety of formats.

Our cross-platform approach allows us to provide medical professionals with a variety of methodologies through which they can learn. From satellite broadcasts to independent medical education forums (IMEFs) to dinner meetings and live symposia at major congresses, our activities are designed to deliver the most effective educational message to the learner.

Independently owned and operated, PAR, also known as Psychological Assessment Resources, was founded in 1978 by R. Bob Smith III, PhD and his wife Cathy to fill a void in the development and distribution of psychological assessment instruments. Over the years, the company has earned a reputation for providing Customers with superior quality assessment instruments and unrivaled Customer Service. Today PAR publishes psychological assessment instruments, software, books and other related materials in the following areas: personality/counseling, neuropsychological assessment, forensics, achievement/development/learning, intellectual/ability/cognitive, behavior/health, and career development/business.

Paradigm Clinical Research has been conducting clinical research for over five years with leading pharmaceutical companies in the world. Our highly experienced staff with their dedication to quality research is paramount to our success. Paradigm Clinical Research has four locations throughout Arizona and California. Our newest location, a phase one facility at the corner of Flowing Wells and Prince Road (1324 W Prince Rd.) is the largest and premier research facility in Tucson.

Pearson is an international media company with world-leading businesses in education, business information and consumer publishing. We help children and adults to learn, business people to make good decisions, and readers to wise up or wind down with a good book. Our businesses fuel the growing demand for effective education and high-quality information in the global knowledge economy, and share a common goal: to help people get on in their lives through education. With 37,000 employees based in more than 60 countries, we aim to serve the citizens of our brain-based economy wherever and whenever they are learning - old or young, at home or school or work, in any pursuit, anywhere. Pearson is listed on the London and New York stock exchanges (UK: PSON; NYSE: PSO) and in 2009 we had sales of £5,624m and operating profit of £858m.

Pensacola Research Consultants is a dedicated clinical research site serving northwest Florida and south Alabama. We take great pride in producing our sponsors with accurate clinical data on time. PRC is dedicated to the advancement of the medical community through the quality management of clinical trials. We achieve this by maintaining a strong standard of ethics in all of our business practices. Acting as an outlet for the pharmaceutical and biotechnical community to access qualified patients, we are able to provide physicians the opportunity to explore promising new treatments while granting the access of these therapies to our community.

Our mission is to improve health care locally and globally by managing clinical trials in a prompt, efficient manner and to the highest quality standards. We treat our customers - Pharmaceutical Companies, CROs, investigators and their clinic staff and patients, as well as our employees with the utmost respect and professionalism. We provide the best possible experience for our customers during the clinical trial process and accept no excuses for less than outstanding service and resolution to all issues – predicted or unforeseen. Pharmaceutical Research Organization works hand-in-hand with the study sponsor and their representatives, Institutional Review Boards, Investigative Sites, and patients to facilitate a smooth clinical trial process from onset to completion.

PRI is an internationally recognized research organization with expertise in pharmacological and multidisciplinary research. Our staff is experienced in the fields of psychiatry, cardiology, rheumatology, family practice, neurology, ophthalmology, gerontology, pharmacoeconomics and quality of life measures. Diagnostic categories treated have included adult attention deficit hyperactivity disorders (ADHD), age-associated memory impairment, Alzheimer's disease, anxiety, arthritis, cataracts, depression, diabetes, glaucoma, hypertension, insomnia, intermittent claudication, migraine headaches, multiple sclerosis, obesity, obsessive compulsive disorder, pain, panic disorder, persistent developmental stuttering, post-traumatic stress disorder, presenile dementia, nicotine addiction (smoking cessation), social anxiety disorder, ulcers and vascular dementia. The research personnel includes several medical directors, each is board certified. Additional personnel includes physicians functioning as co-investigators within their area of expertise, an executive director, research administrators, nurse practitioners, clinical nurse specialists, registered nurses and research assistants. The staff works in collaboration with a multiplicity of professional consultants specializing in psychiatry, rheumatology, gastroenterology, family practice, clinical psychology, internal medicine, endocrinology, cardiology, ophthalmology, computer technology and social sciences, in an effort to provide responsive and responsible medical/psychiatric care within a research environment.

PharmaSeek is an Investigative Site Network (ISN) that specializes in expediting clinical trials to a successful completion. We accelerate the complex process of securing investigative sites for Phase I through Phase IV clinical trials. Clinical research is the longest and most expensive stage of drug development. Effective site selection and patient recruitment can streamline the approval of a drug or device and get it to market quickly. Pairing clinical studies with appropriate sites is critical to achieving successful results. Most clinical trials are delayed at some point. According to CenterWatch, these delays typically result from lengthy contract and budget negotiation, patient recruitment, and regulatory issues. To quickly advance a clinical trial, Sponsors and Contract Research Organizations (CROs) work with PharmaSeek to streamline the site identification and initiation process. Our unique project management methodology provides significant financial value through efficient management of multiple independent sites from a single point of contact.

Prism Research wants to be our client’s first choice for research services. We accomplish this by considering our client a partner for their trial objectives. Prism Research is committed to providing timely and accurate trials. It is our staff’s passion for making a difference that allows us to meet and exceed our client’s expectations. Prism Research is a phase I-IV, 52 bed, clinical trial site located in the heart of the Minneapolis / St. Paul metropolitan area. We are strategically located in a community of over 3 million residents with a rich tradition of medical care advancements. We offer a highly trained dedicated staff, an advanced facility and volunteer database to ensure your trial expectations are met or exceeded.

Protenium Clinical Research is pleased to play an active role in clinical research by conducting FDA approved pharmaceutical studies in a broad range of therapeutic areas for many industry-leading pharmaceutical companies and clinical research organizations. We have made this website available in order to provide information about our current studies, our new research facility as well as our history and experience in clinical research. After moving to our present location in June 2008, Protenium Clinical Research is capable of conducting clinical research in Phase I studies!

For over thirty years, Pulmonary Associates of Richmond has provided a comprehensive range of high-quality, individualized services based upon a commitment to combine compassionate care with advanced education and proven state-of-the-art techniques. PAR physicians are board certified in Pulmonary Medicine, fellowship trained in Critical Care Medicine, and serve as consulting physicians to patients who are very ill and suffer from multiple health issues. Our practice is dedicated to the evaluation and treatment of patients with acute and chronic lung disorders. We also direct and monitor the care of patients who are critically ill. As sleep disorder physicians, we provide care and treatments that lead to more restful and invigorating sleep. We treat conditions that lead to excessive snoring and can be indicators of serious medical conditions, such as sleep apnea.

Training expertise and services that ensures Investigator/Site compliance with FDA requirements for ‘site training’ programs: cooperative groups, sites, SMOs, site networks, hospitals and academic medical institutions. Services offered include: GCP training, Clinical Research Coordinator training, SOP training, Training Plans and Training Records development, implementation and maintenance.

Quality of Life Medical & Research Center (QLM&RC) is a premier research facility located in Tucson, Arizona. Our research clinic has conducted 80+ clinical trials. Our facilities and staff are qualified to handle a wide variety of Phase 1-4 studies, ranging from one to 1000 study participants. Our research patient population includes a cross section of ethnic backgrounds, ages and medical conditions.

Mission: To support innovative clinical research and provide quality clinical research services to the physicians and citizens of our local communities. Regional Health is the only health care system in western South Dakota that serves a 38-county region. Regional Health serves residents from western South Dakota, southeastern Montana, northeastern Wyoming, southwestern North Dakota, and northwestern Nebraska. Regional Health has made a commitment to expand its involvement in clinical drug and medical device research by establishing a separate department for research known as Regional Health Clinical Research (RHCR). This department is devoted to providing complete coordination of Phase II – Phase IV clinical research studies. We offer professionals with experience in working with clinical trials to ensure timely enrollment of patients and strict compliance with protocols and documentation.

RCRC Independent Review Board has been a trusted and leading provider of professional IRB services for 25 years. RCRC provides IRB review for all phases of research in a variety of therapeutic areas and study designs in the pharmaceutical, biotech and medical device industries, and for single-site, multi-site and mega trials. We also provide ethical review for behavioral and social sciences research including, data collection, repository, surveys, outcomes and registries. We offer multiple meetings weekly with a 24-48 hour turnaround time employing 21 CFR Part 11compliant innovative technologies. RCRC developed SafeSync™ Online Submissions with 256-bit public key encryption and GlobeSync™ Virtual Workspace, a WEB-based document management portal allowing 24/7 secure access to IRB study documents.

RDP Clinical specializes in building highly experienced project monitoring teams that are a custom fit for your specific study demands/ needs that are geographically positioned in direct proportion to the site locations to maximize efficiency. We utilize many of the best practices of a functional outsourcing model combined with supportive elements of traditional outsourcing, including but not limited to, a therapeutically aligned Investigator Database, Clinical SOP's, CTMS, GCP Auditing, Travel Policies, and Pass Through Expense Processing.

Biopharma Informatic, Inc dba Research Consultants, is a group of dedicated and experienced investigators based in Texas, Alabama and Florida. We are the link connecting pharmaceutical and contract research organizations to investigator sites and caring individuals seeking to contribute in the advancement of medicine. We work with several qualified physicians with a diverse range of specialties and have conducted a wide variety of studies with successful enrollment targets. Our team of coordinators are highly educated and trained in medicine and research include medical graduates.

The Research Foundation for Mental Hygiene, Inc (RFMH) is a private, not-for-profit membership corporation organized in 1952, for the purpose of assisting and enhancing the research and training objectives of the New York State Department of Mental Hygiene and its component agencies; the Office of Mental Health (OMH), the Office for People with Developmental Disabilities (OPWDD) and the Office of Alcoholism and Substance Abuse Services (OASAS). By way of Columbia University Medical Center - Training for the C-SSRS is available on-line (and indicated/preferred for clinical practice) before administering the C-SSRS. Training can be administered through a 30-minute interactive presentation followed by a series of patient case scenarios for you to score after the training. Those completing the training are certified to administer the C-SSRS, and will receive a training certificate. The training certificate is valid for two years.

The Sall Research Medical Center is a medical clinic that specializes in advancing medical care through research.Dr. Kenneth Sall is the owner of the Sall Research Medical Center and a Board Certified Ophthalmologist with a fellowship in Cornea and External Disease. He has been in practice in the Bellflower/Cerritos/Artesia communities since 1985 and conducting research clinical trials since 1991.During that time over 40,000 patients have trusted Dr. Sall with their eye care. Here are a few of his areas of expertise:

The Scottish Intercollegiate Guidelines Network (SIGN) was formed in 1993. Our objective is to improve the quality of health care for patients in Scotland by reducing variation in practice and outcome, through the development and dissemination of national clinical guidelines containing recommendations for effective practice based on current evidence.

SDS Clinical Trials can improve the efficiency, quality, and safety of your clinical trial with onsite dedicated services. Our specialty, at SDS Clinical Trials, is providing sponsors and CROs with rapid study enrollment, high subject retention, meticulous data and meeting critical timelines. By utilizing a central IRB combined with our 100,000+ patient database, our energetic and experienced, bi-lingual staff ensures SDS Clinical Trials will meet and exceed goals efficiently.

Exactly what is it that we do at SGS? We make business faster, simpler and more efficient, giving our clients a real competitive edge in the area of inspection, verification, testing and certification. SGS is the world's leading inspection, verification, testing and certification company. Recognized as the global benchmark for quality and integrity, we employ 59,000 people and operate a network of more than 1,000 offices and laboratories around the world. Experts in Clinical Development: The Clinical Research team provides integrated solutions from preclinical activities to Phase I-IV trials and bioanalytical testing. SGS Life Science Services represents the largest network of contract testing laboratories, with 14 laboratories in 12 countries, offering comprehensive a portfolio for the analysis of raw materials, APIs, excipients and finished products.

The 2011 SharpBrains Summit is designed to help innovators, decisionmakers, researchers and all professionals in the brain health and cognitive fitness field who want to

1. learn about the latest market trends, technologies, needs and opportunities,

2. discuss emerging research and best practices,

3. meet and share notes with colleagues who face similar priorities and challenges, and

4. interact with a crosssector group of industry, technology and research innovators who are changing the way things are done.

You will be among a select group of talented professionals representing the premier research sites. Who attends? Top-tier site decision-makers. Our group is diverse, and just the right size to foster one-on-one exchanges and small group discussions. You will meet study sponsors and CRO decision-makers. They attend the Summit to connect with the best sites and that's precisely what they find. The Summit sets the stage for relationship-building and new business partnerships. They come to meet you and send their site selection decision makers. You will come away with real-world solutions for your business challenges - plus tools to use immediately that will improve your work life every day.

SP Research P.L.L.C. is a full service research site with a comfortable waiting room; spacious laboratory room with exam table, electronic sphygmomanometer, centrifuge, -20 Freezer, and other amenities. The site also boasts a double locked, temperature-controlled room for study medications, a designated space for study monitors with internet accessibility, telephone and privacy. SP Research PLLC is centrally located in The Oil Center off of Northwest Expressway, with accessible parking behind the buildings. The research site is located on the 6th floor of the west tower in suite 602W, right next door to the PI’s private practice, insuring close proximity and the availability of MD’s during normal working hours.

We study medication-based treatments for various physical and emotional conditions. Some of these studies are undertaken to enhance our understanding of currently available medications (for example, determining optimal dose schedules). We also conduct research on medications that are not yet available, and look at questions of expanded usage (for example, determining whether an established medical treatment for depression is also effective in treating anxiety). All medications now on the market have gone through this same process. Many of our studies involve comparisons between a study medication, a commonly prescribed medication, and a placebo (inactive substance). We include placebo groups in some of our studies because a surprising number of people improve when treated with placebos, and the status of patients in the placebo group gives us a comparison base for evaluating the effectiveness of active medications. Our goal is to expand what is known about medical treatment while offering top-quality patient care. Our patients receive all research care, mental health evaluations, medical evaluations, and supervision by our professional and experienced staff. A post study treatment program is also available to patients once their study participation has been completed. All of these services are provided at no cost to the patient.

Transportation Compliance Associates Inc., is an international hazmat training and consulting company which is dedicated to quality hazardous materials training. We provide on-site as well as on-line, customized hazardous materials and dangerous goods training for DOT, IATA, IMDG, and TDG-Canada customized to the products you ship. Customized does not mean more expensive. It means better understanding, higher retention of concepts and a more superior quality of training.

ACTHIV is state-of-the-science conference for frontline health care professionals, in scientific collaboration with multiple federal and independent agencies. The conference is designed for all frontline clinicians providing HIV care for various population groups.

We are a full-service consulting firm for medical professionals, specializing in office automation, transcription, and clinical trial management. Our clinical trial management services include the startup and management phase II-IV trials. We offer complete training and ongoing support for new physicians and study coordinators. We currently have ongoing trials for cardiovascular, dermatology and endocrinology. Our expert staff manages regulatory, patient recruitment and source documents. Additionally, The Bracane Company offers Legal Nurse Consulting for Health Care, Medical Malpractice, Personal Injury, Product Liability, and Workers Compensation. The Bracane Company provides screening and review of cases for merit, review of medical records, definitions for standards of care and access to expert witnesses.

The Dermatology Clinical Research Center of San Antonio™ is an independent clinical research site specializing in dermatology clinical trials. The Center was founded by Steven A. Davis, MD in 1987. It has its own full-time staff and dedicated exam rooms and offices immediately adjacent to Dr. Davis's clinical practice, the Dermatology & Laser Center of San Antonio™. The practice provides a full range of dermatology medical, surgical, and cosmetic services and records over 15,000 patient encounters a year.

Since our Research Center is dedicated exclusively to dermatology, our staff has vast experience in dermatology-related conditions, plus a large database of both diagnosis-coded clinical patient lists and previous clinical study patients, giving us the ability to deliver accurate data in a timely fashion. Compliance and completion rates for our studies are high. Enrollment and completion rates typically meet or exceed sponsor requirements and we are often asked to enroll more than our original quota to help the sponsor reach its national goals.

The Geneva Foundation is a private, non-profit organization created in 1993 with the sole purpose to support and promote the advancement of military medicine. The organization remains steadfast to providing quality services to military medical researchers and excellence in education and training programs nationwide. Geneva accomplishes this daily through the dedicated efforts of highly skilled, experienced employees with an emphasis on quality work, efficiency and superior customer service. Geneva continues to build on its successes and is recognized as a leader in providing comprehensive services to military medical personnel. The Geneva Foundation provides management and administrative expertise in the areas of federally funded research grants and contracts, privately funded clinical trials and investigator-initiated studies, and medical education and training programs.

The RAN Institute's mission is to provide excellence in clinical research education. We provide GCP and Clinical Research Training tools including: GCPs Made Easy® Flash Cards Step-by-Step Clinical Research Guides for Investigators, Coordinators, Sponsors and Monitors On-line GCP Training with and without CE credit On-line Informed Consent Training Certification Preparation Packages.

TRIALOGIC is a Clinical Research Management Organization whose sole purpose is to support the successful outcome of clinical trials for the pharmaceutical, biotech, and medical device industries. We take the mission of every Sponsor seriously and are committed to providing quality data, at its best. Each day we work to earn recognition as a company that provides its customers with unparalleled service and results. Trialogic is comprised of two primary divisions; Site Management and Trial Management. Working on both sides of clinical trials, we manage clinical research sites in behalf of Principal Investigators and we manage clinical trials in behalf of study Sponsors.

UCLA Comprehensive Stroke Center is Recognized as one of the world's leading centers for the management of cerebral vascular disease, the UCLA Stroke Center treats simple and complex vascular disorders by incorporating recent developments in emergency medicine, stroke neurology, microneurosurgery, neuroanesthesiology, and rehabilitation neurology and more.

El objetivo de esta alianza es formar a futuras generaciones de profesionales de la salud y colaborar con el desarrollo de su cuerpo médico, dado que la Facultad otorga a los especialistas de la Clínica la posibilidad de realizar investigaciones y ejercer en docencia. Cuenta con las escuelas de - Medicina - Odontología- Enfermería - Fonoaudiología – Kinesiología - Nutrición y Dietética - Tecnología Médica y Postgrados en Medicina en el Campus de Las Condes y en el en Campus San Carlos de Apoquindo de la Universidad del Desarrollo. La misión principal es formar profesionales de excelencia, con una sólida base científica, humanista y social.

Situated on a 20-acre campus in the Washington Heights community of northern Manhattan and comprising roughly half of Columbia University's nearly $3 billion annual budget, Columbia University's Medical Center provides world-class leadership in scientific research, health and medical education and patient care. Faculty members from its four schools (College of Physicians & Surgeons, College of Dental Medicine, School of Nursing, and Mailman School of Public Health). Carry out the school's core mission of educating and training future generations of health care professionals. Conduct basic research with the ultimate goal of translating discoveries into new techniques for fighting disease and improving health. Are responsible for a number of significant clinical breakthroughs - among them, the first blood test for cancer, the first medical use of the laser, and the first successful transfer of genes from one cell to another.

The University Medical Center Hamburg-Eppendorf is the largest among Hamburg's hospitals with approximately 1460 hospital beds. Each year the medical center treats around 80 000 in-patients. Additionally, approximately 260 000 out-patients as well as 113 000 emergency patients are treated. Similar to most university hospitals, the UKE offers a complete range of treatment options for patients. At the same time, new ideas in research and new approaches for the diagnosis and therapy of diseases are applied. The range of medical care extends from overall diagnostic service to highly specialised and complex treatments necessary for uncommon diseases. For the Hamburg region, a large number of therapies and complicated surgical procedures, especially in the field of transplantation (heart, liver, kidney as well as bone marrow) can only be performed in the UKE.

Our mission is to undertake leading-edge, internationally-competitive research while offering a challenging student-centred learning environment. Through our status as a leading international university, we aim to sustain and add value to Scottish culture and society, to the natural environment and to the national economy.

Oxford University Press is a department of the University of Oxford. It furthers the University's objective of excellence in research, scholarship, and education by publishing worldwide.

The University of Porto provides almost 500 training programs (1st, 2nd and 3rd cycles of continuous training), covering such diverse areas of knowledge as life sciences, engineering, technological innovation, humanities, social and cultural studies and artistic creation. To achieve this, the University of Porto has a qualified and specialized body of 1,830 ETI staff members, of whom 1,313 hold doctorates.

Studenti, docenti, personale interno e visitatori possono acquistare originali portapranzo, felpe, cappellini, grembiuli da cucina, matite, agende, ma anche oggetti tecnologici come pen drive e penne laser, reinterpretati dagli studenti dei corsi di laurea in Disegno industriale. Prossimamente sarà possibile ordinare gli articoli anche attraverso il sito dedicato, già attivo sulla home page dell’Università.

VirtualScopics is a leading imaging core lab providing central reads and quantitative imaging solutions for drug and medical device clinical trials. Therapeutic area expertise includes: oncology, rheumatoid arthritis, osteoarthritis, neurology, and cardiovascular studies utilizing MRI, PET, CT, Ultrasound, and X-Ray imaging modalities.

Advanced semi-automated analysis software is used in conjunction with expert technicians and radiologists to quantify image-based biomarkers to deliver precise and repeatable measurements. This delivers the opportunity for compressed trial time, reduced subject sample size, real-time reads and the ability to prove drug or device efficacy earlier.

We provide an unparalleled depth of experience, technological capability and expertise in imaging for clinical trials. Our services support all aspects of imaging in clinical trials, from design to FDA submission, pre-clinical through Phase IV. We are a company with a commitment to customer service that far surpasses what our customers expect. We respond quicker, foresee challenges sooner, and get you the answers you need faster—all in a manner that gives you a deep sense of trust and confidence.

VHI has been in the business of providing exercises and information for fitness and health professionals since 1980. The company was formed by John E. and Ann C. Beaulieu in Springfield, Oregon. In 1985 they moved the company to its present location, Tacoma, Washington. VHI strives to produce educational materials of the highest quality. Professionals in the fitness and health care fields use these materials to create handouts for their clients and patients. These handouts will assist the client/patient with home exercise routines or provide additional information as follow-through to their visit with the professional.