Interview: From Regulatory Compliance to Patient Recruitment: Understanding Clinical Trials in India
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Interview: From Regulatory Compliance to Patient Recruitment: Understanding Clinical Trials in India
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Join host Dr Andreas Grund as he discusses the ins and outs of conducting clinical trials in India with industry expert, Dr Deepa Arora. They unravel the Indian regulatory environment, highlight the impact of diversity in clinical studies, and explore India's significant role as the 'pharmacy of the world.' Deepa provides valuable insights into the benefits and challenges of performing clinical trials in India, emphasizing the country's compliance with international guidelines and the quality of data produced. This enlightening discussion is a must-watch for anyone involved in pharmaceutical research considering India for their clinical trials. Don't forget to like, comment, and subscribe for more expert perspectives on the world of clinical trials.
