Human Subject Research (NIH)Easy to read website, written for individuals or groups looking into human subjects research for the first time.
IFPMA Clinical Trials PortalComplete information database on current and completed clinical trials of member companies of the International Federation of Pharmaceutical Manufacturers & Associations.
CanadaTrialsCanadaTrials.com is a public source of information for patients, families and physicians, listing a searchable database of Clinical Research Trials that are actively enrolling patients in Canada. In addition CanadaTrials.com offers the latest Medical and health news with links to the most authoritative information sources updated hourly, and links to general health information and patient support groups.
CanadaTrialsCanadaTrials.com is a public source of information for patients, families and physicians, listing a searchable database of Clinical Research Trials that are actively enrolling patients in Canada. In addition CanadaTrials.com offers the latest Medical and health news with links to the most authoritative information sources updated hourly, and links to general health information and patient support groups.
Drug Industry Document ArchiveThe Drug Industry Document Archive (DIDA) contains over 2500 documents about pharmaceutical industry clinical trials, publication of study results, pricing, marketing, relations with physicians and involvement in continuing medical education.
Most of these previously secret documents were made public as a result of lawsuits against the following pharmaceutical companies: Merck & Co., Parke-Davis, Warner-Lambert, Wyeth, and Pfizer.
Consolidated Standards of Reporting Trials (CONSORT)CONSORT, which stands for Consolidated Standards of Reporting Trials, encompasses various initiatives developed by the CONSORT Group to alleviate the problems arising from inadequate reporting of randomized controlled trials (RCTs).
The main product of CONSORT is the CONSORT Statement, which is an evidence-based, minimum set of recommendations for reporting RCTs. It offers a standard way for authors to prepare reports of trial findings, facilitating their complete and transparent reporting, and aiding their critical appraisal and interpretation.
The CONSORT Statement comprises a 25-item checklist and a flow diagram, along with some brief descriptive text. The checklist items focus on reporting how the trial was designed, analyzed, and interpreted; the flow diagram displays the progress of all participants through the trial.
HIPPA/Privacy Rule & Vulnerable Populations Web Sites
HIPPA information (NIH)The Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule is the first comprehensive Federal protection for the privacy of personal health information. Research organizations and researchers may or may not be covered by the HIPAA Privacy Rule.
Association of Clinical Research Professionals"Whether you are looking for a new job, or ready to take the next step in your career, we'll help you find the opportunity that is right for you. ACRP's Career center is the best place to find jobs in the clinical research field. You can browse hundreds of jobs posted by top-quality employers while keeping your resume online for employer review. You can also create a job agent that will seek out jobs tailored to your interest, and alert you immediately when those jobs are posted in the Career Center." (from web site description)
Duke Clinical Research InstituteAs part of the Duke University School of Medicine, the Duke Clinical Research Institute is known for conducting groundbreaking multinational clinical trials, managing major national patient registries, and performing landmark outcomes research.
The Clinician-Consumer Health Advisory Information Network (CHAIN)The Clinician-Consumer Health Advisory Information Network (CHAIN) is an online educational, informational, and resource dissemination program operated as a collaborative effort of the Centers for Education and Research on Therapeutics (CERTs) Educational Consortium.
Fraud and Misconduct in Research by 
Intelligent Drug Development: Trials and Errors in Clinical Research by 
Making Meaning of Data in Pharmaceutical and Clinical Research by 
Principles and Practice of Clinical Research by 
