Clinical Research: 8 Essential documents that you should know.

Hello there, in this video we will be looking at some of the essential documents required in clinical trials. This is the most important topic for all pharma students. Below are the topics we are going to discuss in this video: What are the documents required in CLinical research What is a Protocol? What is Informed Consent form? What is Case report form What is a Clinical study report? What is Trial Master File? What is Investigator's Brochure? and many more I would highly recommend you to watch the whole video, but please use the chapters for better navigation if you can't. 01:29 Document 1 [CDA (Confidentiality Agreement)] 02:40 Document 2 [Protocol] 04:16 Document 2 [Investigator’s Brochure] 05:47 Document 4 [ICF (informed Consent Form)] 07:28 Document 5 [CRF (Case Report Form)] 09:16 Document 6 [CSR (Clinical Study Report)] 10:20 Document 7 [TMF {Trial Master File)] 11:35 Document 8 [Source Document] If you have any doubt you can DM me on   / edu.chemipro     / chemipro_   Antihypertensive series:    • क्या हैं ACE INHIBITORS जानिए आसान भाषा मे...   Formation of urine:    • Nephron structure and function (IN HINDI)|...   #pharmacology #chemipro #pharmacologyinhindi #pharmacy #medicine #clinicalresearch