Clinical Research Record Retention Guidelines
from Emergent Epidemics Research with Dr. Amos Ndhere Hosted by Amos Ndhere MD, MS
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 ****** 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 📈. ****** 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 ****** PS - Join the conversation on social https://www.linkedin.com/in/amosndherehttps://twitter.com/amosndherehttps://facebook.com/amosndherehttps://www.instagram.com/amos.ndhere/Clinical Research #clinicalresearch #clinicaltrials #Africa #publichealth #gcp
Embed this episode
No transcript yet.