Clinical trials in India
Clinical Trials Registry - India (CTRI)
A free and online public record system for registration of clinical trials being conducted in India that was launched on 20 th July 2007.
Why are clinical trials necessary in India? - PMC
Clinical trials are emerging as an important activity in India as it is an essential component of the drug discovery and development program to which India ...
Clinical Research Regulation For India | ClinRegs
The Central Drugs Standard Control Organization (CDSCO) is the regulatory authority responsible for clinical trial oversight, approval, and inspections in ...
Clinical trials in India - Wikipedia
Various government agencies and laws regulate clinical trials. The Drugs Controller General of India grants approval for clinical trials and is the top level ...
Global Focus: Clinical Trials in India - Food and Drug Law Institute
These mandatory guidelines cover all biomedical research in India at all stages of drug development, whether prior to or subsequent to product registration in ...
Cancer Trials Ecosystem in India—Ready for Prime Time?
Although only 44 trials were registered from 2002 to 2004, there were 1,548 trials registered between 2005 and 2010. The financial value of ...
Search, Clinical Trials Registry - India (CTRI)
Search for trials: Prospective/Retrospective Trials: Prospective Retrospective Type of Trial: Observational Interventional PMS BA/BE Month and Year of trial ...
Government of India · Home · Clinical Trial · Clinical Trials ...
Complexity of clinical trial operationalisation in India - The Lancet
Ethics committees in India face several challenges, such as lack of adequately trained staff, extensive workload, inadequate space allocated for operations,
The Evolving Regulatory Landscape for Clinical Trials in India
While several of the new rules seem untenable in clinical research, over the past several years the Indian government has made an attempt to clarify and refine ...
Clinical Trials in India: History, Current Regulations, and Future ...
The Indian clinical trial market had started flourishing after the amendment of the patent law and Schedule Y of Drug and Cosmetic Rules in 2005 ...
Clinical Trials and Biomedical Research in India
The history of clinical research regulation in India can be traced back to the. Drugs and Cosmetics Act, 1940 (“DCA”) - India's primary drug control legislation ...
A research study involving human volunteers (also called participants) that is intended to add to medical knowledge. There are two types of clinical studies: ...
Landscape of cancer clinical trials in India - The Lancet
This study aims to depict the evolving landscape of cancer clinical trials in India by analysing the clinical trials registered in Clinical Trial Registry- ...
Why did the DCGI of India cease clinical trials on NCES in India
It costs about $2,000 to track the progress of a single Indian patient in a clinical trial, GlaxoSmithKline. CEO Jean-Pierre Garnier wrote in the May 2008 ...
Clinical Trials in India | Pfizer India
Clinical trials in India are conducted for Pfizer's Global Pipeline Products in Oncology, Vaccines, Rare Disease, Infectious Diseases, Inflammation and ...
Clinical Trials in India - ScienceDirect
Clinical trials in India are conducted under the legislation contained in Drugs and Cosmetics Act, 1940 and Drugs and Cosmetics Rules, 1945. The clinical trial ...
Find out about our clinical trials process in India, how we work with doctors and volunteers throughout this process, and how to become a research volunteer in ...
India - GCT - Global Clinical Trials
The Drugs Controller General of India (DCGI), an official of the CDSCO, is the final regulatory authority for the approval of clinical trials in the country.
India's New Drugs and Clinical Trials Rules: An Industry Perspective
... the recently published, revised regulatory pathway in India and focuses on the regulatory changes and their impact on industry and on clinical trials.