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The Declaration of Helsinki is a set of ethical principles and guidelines for conducting medical res...
Basics of Clinical Data Management
Investigator roles
INVESTGATIONAL NEW DRUG APPLICATIONS
INVESTIGATOR'S BROCHURE as per ICH E6 (ICH GCP)
The landscape of clinical trials is intricate, involving extensive data collection, management, and ...
Guidelines for clinical trials
Schedule Y
Cls
Quality Assurance and Quality Control in Clinical Research
No research without action,no action without research.
clinical trails
Passive surveillance
A presentation on INFORMED CONSENT FORM which is easy to understand and easy to explain and in very...
For better understanding of students. This will give you a detailed explanation of IND APPLICATION. ...
“CSR is a detailed regulatory document which gives the information about the methods and results (...
This trial describes the use of Aspirin or Clopidogrel as a monotherapy after percutaneous coronary ...
Institutional Ethics Committee
CLINICAL TRIAL REGISTRY OF INDIA
Clinical data management (CDM) is a critical component of clinical research, involving the collectio...
This PPT give information about Institutional Human Ethics Committee
ICH GCP guidelines
