South African Regulatory Framework for Clinical Trials

Ever wondered how clinical trials in South Africa are regulated to ensure they’re safe, ethical, and effective? In this video, I break down the role of the *South African Health Products Regulatory Authority (SAHPRA)* and the ethical guidelines that protect trial participants and uphold scientific integrity.
Here’s what you’ll learn:
✅ What is SAHPRA, and why is their approval essential for clinical trials?
✅ The role of *Research Ethics Committees (RECs)* in safeguarding participants.
✅ The importance of *informed consent* and transparency in trials.
✅ How South Africa’s ethical standards align with global best practices, making it a trusted hub for medical research.
Whether you’re a student, researcher, or just curious about how new treatments are developed, this video gives you a clear understanding of the regulatory process that ensures trial integrity.
💡 Found this insightful? Don’t forget to *LIKE**, **SUBSCRIBE**, and **SHARE* this video with anyone interested in science or healthcare!
💬 Join the conversation: What aspect of clinical trial regulation do you find most important?
#SAHPRA #ClinicalTrials #MedicalResearch #EthicsInScience #HealthcareInnovation