KNOW ABOUT THE ETHICS COMMITTEE REGISTRATION https://www.articlealley.com/news/ethics-committee-registration-ec-registration-cdsco-process-cost-82860 Ethics Committee (EC) Registration is a mandatory regulatory requirement for institutions, hospitals, and independent ethics committees that are involved in clinical trials, biomedical research, or bioavailability/bioequivalence studies in India. The registration is granted by the Central Drugs Standard Control Organisation (CDSCO) under the Drugs and Cosmetics Act, 1940, and the New Drugs and Clinical Trials Rules, 2019. #cdscoregistration #drugs #license #ethicscommittee

Retatrutide UK Legal Status: Debunking the “31 October 2025 Ban” Rumour However, as always – selling any unlicensed medicine for human use in the UK is illegal, and Retatrutide remains an investigational drug only legally obtainable via approved clinical trials. https://vitalitypeptides.co.uk/retatrutide-uk-legal-status-2025/

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Medical Affairs Clinical Trials Medical Affairs Leadership in Rare Diseases In the complex tapestry of healthcare, the domain of rare diseases represents a frontier laden with both grave challenges and profound opportunities. Medical affairs leadership plays a pivotal role in transforming clinical trials and the development of rare disease therapies. For more info: https://www.zs.com/insights/the-pivotal-role-of-medical-affairs-in-rare-disease-leadership

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Clinical Trial Performance Management and Insights Using CRM Clinical trials face delays and operational challenges due to fragmented communication and repetitive tasks. Implementing CRM in clinical research centralizes critical trial data, enhances coordination, and streamlines management processes. For more info: https://www.zs.com/insights/crm-for-clinical-trial-site-engagement

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