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The top documents tagged [investigational products]
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investigational products
Clinical trials: Terminology
2.142 views
Differences in OHRP, FDA and ICH Regulations/Guidelines Monika Haugstetter, MHA, MSN, RN Human Subject Protection Office (HSPO) and Institutional Review.
213 views
Regulatory Submission Process Clinical Study Application: 1. Submit an appointment requestappointment request 2. Fill one of the three templates: - BE.
214 views
Human/animal use considerations. Protection of Human Subjects Basic principles Basic principles –Clinical trials should be conducted in accordance with.
214 views
McLeod Health Speakers Faculty Disclosure / Unlabeled Uses Disclosure Speakers Faculty Disclosure Unlabeled Uses Disclosure Coy Irvin, MD No relevant financial.
219 views
II French-Chinese Bioethics Workshop Paris 22, 23 February 2007 Jiali LI, MD, Ph.D Cancéropôle Île de France (Cancer Agency of Paris Area)
216 views
11 IND-Enabling Safety Studies for Rare Diseases Timothy J. McGovern, Ph.D. ODE II Associate Director for Pharmacology/Toxicology September 16, 2014 1.
220 views
ADR Monitoring and Reporting in Clinical Trials
96 views
Ich gcp e6 r1 _guideline
2.479 views
FDA Advisory Panel Miltenyi Biotec CliniMACS ® CD34 Reagent System September 23, 2011 With Sincere Thanks and Appreciation To:
220 views
Quality Systems Compliance Assessment
34 views
All noxious and unintended responses to a medicinal product related to any dose should be considered adverse drug reactions.
219 views
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