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Keywords: clinical trial approval in India, DCGI, ICMR guidelines, ethics committee Clinical trials are the backbone of medical innovation, playing a crucial role in bringing new drugs, vaccines, and medical devices to the market. But before a single participant is enrolled, the proposed study must pass through a robust approval process that ensures ethical integrity,…

Keywords: informed consent, clinical trial ethics, patient rights in trials, consent form Blog Content: Informed consent isn’t just paperwork — it’s a crucial dialogue between researchers and participants. **What is Informed Consent?**It’s a voluntary agreement where the participant is fully informed about the trial’s purpose, risks, benefits, and their rights. **Key Elements of Informed Consent:**–…