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2. Certified IRB Professional - Wikipedia

   en.wikipedia.org/wiki/Certified_IRB_Professional

   Created in 1999, the CIP program is a result of many years of discussions and planning by organizational members and leaders. It is endorsed by federal regulatory officials, professional associations, many national advisory bodies and IRB professionals who are committed to improving the quality of human research protection programs.

3. Clinical research associate - Wikipedia

   en.wikipedia.org/wiki/Clinical_research_associate

   A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.

4. List of clinical trial registries - Wikipedia

   en.wikipedia.org/wiki/List_of_clinical_trial...

   The DRKS is an open access, free of charge online register for clinical trials and is available both in English and German. DRKS is part of the WHO's ICTRP. The DRKS works with two partner registries in Germany, DeReG (German Registry for Somatic Gene-Transfer Trials) and Clinical Trial Registry of the University Medical Center Freiburg. [4]

5. ePharmaSolutions - Wikipedia

   en.wikipedia.org/wiki/EPharmaSolutions

   ePS was founded in 2001 by Lance Converse and is headquartered in Plymouth Meeting, Pennsylvania, employing 60+ clinical researchers and technologists. ePharmaSolutions' Clinical Trial Portal technology won the 2009 and 2013 Bio-IT World for “Best in Class Clinical Trial Technology” and the 2013 Microsoft Lifesciences Innovation Award ...

6. Clinical trial - Wikipedia

   en.wikipedia.org/wiki/Clinical_trial

   A clinical trial participant receives an injection. Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietary choices, dietary supplements, and medical devices) and known interventions that warrant further ...

7. Trial master file - Wikipedia

   en.wikipedia.org/wiki/Trial_master_file

   In a clinical trial involving human subjects, a set of content known as a trial master file (TMF) must be produced in accordance with applicable international and local regulations. TMFs are a collection of documents and other artifacts which "individually and collectively permit evaluation of the conduct of a trial and the quality of the data ...

8. AOL Mail

   mail.aol.com

   Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

9. Critical Path Institute - Wikipedia

   en.wikipedia.org/wiki/Critical_Path_Institute

   In the interest of national and global public health, C-Path develops large databases of aggregated clinical trial data that can be used to study disease progression. These data are also used to develop and qualify biomarkers and clinical outcome assessment instruments that are shared with the greater community for use in drug development. C ...