International Conference on Harmonization (ICH) Good Clinical Practice (E-6) requires investigators and sponsors to retain specific study records associated with the conduct of clinical research.

These documents are often referred to as Essential Documents.

🎥 In this episode, I share insights about clinical research record retention in the context of global health trials. The practices, essentially follows International Conference on Harmonization-ICH GCP Guidelines E-6 section 8

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Hi, I am Dr. Amos Ndhere, a medical doctor, vaccinologist and pharmaceutical product development specialist.I support pharma industry leaders to execute safe, cost-effective clinical trials that accelerate delivery of life-changing treatments to patients and grow emerging market share 📈.

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Hey there! Are you interested in discussing efficient and safe ways to deliver your next global health research? Let's have a chat and explore your options!https://www.aceresearchafrica.com/contact

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