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Pharmacological and Toxicological screening method-II, Mpharm (Pharmacology),1st year, 1st semester
describe about role of sponsor and CRO on clinical trial process
ICH E 6 good clinical practice (GCP)
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
Clinical Data Management (CDM) refers to the process of collecting, cleaning, and managing clinical ...
The complexity of a clinical research trial involves keeping and storing multiple essential document...
there are many clinical trials every day but good reporting of these trials is essential. This talk ...
In any work or process documents that are needed before initiation, Between or generally the end of ...
Lets, just get to know more about safety reporting in clinical trails with some terminologies, repor...
INVESTIGATIONAL NEW DRUG APPLICATION AS PER FEDERAL FOOD DRUG AND COSMETIC ACT
schedule y of drugs and cosmetic acts
Crp
Schedule y
case report form in clinical trail
The term ‘’essential documents’’ refers to the documents which, according to the ICH-GCP Gui...
This presentation provides a comprehensive overview of Good Clinical Practice (GCP), an internationa...
A detailed study of the rules, regulations and guidelines of Good Laboratory Practices that should b...
Good Clinical Practice (GCP) is an international set of guidelines that ensures reliable results and...
Effective radiotherapy treatment requires robust protocol development, ensuring clear treatment para...
Investigational new drug application (ind)
Regulatory Requirements For New Drug Approval. This topic is from Industrial Pharmacy-II, B.Pharm Fi...
ethics committee slides by Dr Satyabrata Sahoo
Good Clinical Practices for drug discovery and development
Investigational Product: procurement, storage, labeling procedures is included in this presentation.
