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Clinical Research Essentials: ICH GCP & Study Designs Series
6th Series - Clinical trial personnel - Roles and responsibilities

6th Series - Clinical trial personnel - Roles and responsibilities

Clinical Research Essentials: ICH GCP & Study Designs Series

محتوى الكورس

جميع الدروس
21 درس
08:46 11th Series - History Pharmacovigilance
01:02 Pharmacovigilance methods #ytshorts
00:54 Establishment Pharmacovigilance Centre #ytshorts
17:59 19th Series - Pharmacoeconomics - Part B
14:12 18th Series - Pharmacoeconomics - Part A
09:34 17th Series - Pharmacoepidemiology
14:09 16th Series - Pharmacovigilance Softwares
15:10 15th Series - National International Pharmacovigilance Scenario - Statistical methods
12:33 14th Series - Passive Surveillance Active Surveillance Vaccine Safety Surveillance
09:31 13th Series - WHO International Drug Monitoring Program & Pharmacovigilance Program of India
09:29 12th Series - International Classification of Diseases & International Nonproprietary Names of Drugs
09:31 1st Series - ICH GCP Guidelines for Clinical research
13:17 10th Series - ADR Spontaneous reporting Predictability and Preventability assessment of ADRs
08:40 9th Series - Terminologies - Detection and Reporting of ADRs
08:41 8th Series - Adverse Drug Reactions ADR
15:34 7th Series - Clinical trial documentation
17:02 6th Series - Clinical trial personnel - Roles and responsibilities
08:28 5th Series - Cross Sectional study
13:06 4th Series - Non-randomized Control Trial and Observational studies
09:02 3rd Series - Institutional Review Board and Randomized Control Trial
08:34 2nd Series - Informed consent