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Patient data privacy is one of the most critical aspects of clinical trials, especially with the inc...
A Presentation about D&C Act 1940 - Schedule Y, Amendment 2005 by Akshay Anand, covering aspects...
Regulatory aspects of clinical trials refer to the rules, regulations, and guidelines set forth by r...
21 CFR Part 50 and 54 are U.S. Food and Drug Administration (FDA) regulations for clinical trials. 2...
This presentation provides an in-depth overview of ethical considerations in biomedical and health r...
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
NDCT STANDS FOR NEW DRUG CLINICAL TRIAL RULE. HERE YOU WILL GET TO KNOW ABOUT THE NDCT RULE HISTORY,...
Overview of clinical trials in medicine
The New Drugs and Clinical Trials Rules, 2019 (NDCT Rules, 2019) apply to all new drugs, investigati...
this slide tells about schedule Y, Good Clinical Practice, CDSCO, Ethics committee, consent form, Se...
clinical trial application in india
schedule y
this ppt covers all quary about the CDSCO ( central drug standard control organisation ,drug control...
An Overview of CDSCO Registration. The CDSCO stands for Central Drugs Standard Control Organisation ...
Here’s a concise description you can use for your clinical trials PPT upload: This presentation p...
Presentation providing brief description of clinical trials, their phases, types, Protocol, developm...
Schedule Y
About the submission of IND, NDA and ANDA.
includes the details of new drug development and different phases of clinical trials
This PPT covers the B. Pharm, Pharmaceutical Jurisprudence Unit-I topics with Objectives, Definition...
a regulatory body of India that conducted trial.
clinical trials history and types
Global submission of IND - Regulatory affairs 1st sem M. Pharm pharmaceutics
