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Clinical trials are critical in the development of novel medications and cures, advancing medical sc...
Regulatory framework of India, Acts and Regulations for conduct of clinical trial in India, Schedule...
This webinar will tell you what you need to know about clinical trials, their history, and help you ...
The mission of the Clinical Trials Registry-India (CTRI) is to ensure that all clinical trials condu...
“CSR is a detailed regulatory document which gives the information about the methods and results (...
Clinical trials are fundamental to the development and approval of new drugs, ensuring their safety,...
A document outlining trial objectives, design, methodology, and analysis plan.��It serves as a r...
IRB/IEC serves as an independent body that reviews, evaluate, approves and decides on the scientific...
A clinical trial is a culmination of the several stages of a drug or medical device development prog...
Recent advances in the pharmacotherapy of Non-Alcoholic Steatohepatitis (NASH) have made significant...
Safety data generation in pre-clinical phase, clinical phase and post approval phase
Regulatory reporting is a fundamental aspect of scientific research and is crucial for ensuring comp...
phases of a clinical trial /oncology
Clinical data management (CDM) is a process that involves the collection, cleaning, and management o...
Study start-up (SSU) is so much more than a one-time document management exercise. It’s a global, ...
clinical trial approaches with clinical trial management under ethics committee
The New Drugs and Clinical Trials Rules, 2019 (NDCT Rules, 2019) apply to all new drugs, investigati...
clinical trial application in india
schedule y
regulatory definitions ,Conduct of the clinical trial
Good Clinical Practice Principle of ICH GCP Institutional Review Board (IRB)/IEC Informed Consent
a regulatory body of India that conducted trial.
In any work or process documents that are needed before initiation, Between or generally the end of ...
