Are you a student or working professional in Drug Regulatory Affairs (DRA) looking to strengthen your understanding of the regulatory landscape for medical products? The Translational Health Science and Technology Institute (THSTI), in collaboration with the Central Drugs Standard Control Organisation (CDSCO) and the World Health Organization (WHO), is offering a free online course titled “Good Regulatory Practices in the Regulation of Medical Products” as part of their regulatory series. Hosted on THSTI’s WHO Learning Management System, this self-paced module is a valuable resource for anyone aiming to bolster the regulatory framework in India and beyond.
Why This Course Matters
Regulatory authorities worldwide strive to ensure the safety, efficacy, and quality of medical products, from pharmaceuticals and biologics to medical devices. Good regulatory practices (GRP) serve as the cornerstone for developing, implementing, and reviewing regulatory instruments—such as laws, guidelines, and inspection protocols—that protect public health and foster industry innovation. By understanding GRP:
Students gain foundational knowledge crucial for careers in regulatory affairs, quality assurance, and compliance.
Professionals deepen their expertise, stay updated on global best practices, and enhance their organization’s ability to meet evolving regulatory requirements.
This particular course, developed jointly by CDSCO, WHO, and THSTI, aligns international guidelines with India’s regulatory framework, making it especially relevant for practitioners in our system.
Course Overview
Upon enrolling, participants will have access to:
Lecture Recording
A comprehensive video lecture covering key principles of GRP, illustrated with real-world case studies.PowerPoint Presentation
Downloadable slides summarizing the lecture, ideal for quick reference and in-house training sessions.Certificate of Completion
Upon finishing the module and acknowledging your understanding, you can download an official certificate noting your mastery of the topic.
How to Enroll
Visit the Course Page
Navigate to the THSTI WHO LMS portal:
https://lms.thsti.in/lms-new-cer/Register or Log In
If you’re new, create a free account; existing users can simply log in.Select the Course
Click on “Good regulatory practices in the regulation of medical products” and hit Proceed.Complete the Module
Watch the lecture, download the slides, and acknowledge your understanding to unlock the certificate.
Enrollment is entirely free—no hidden fees or subscription required.
Implementing What You Learn
In Academia: Integrate GRP concepts into classroom discussions, seminars, and project work.
At Your Workplace: Pilot small-scale audits or process reviews based on GRP checklists.
Within Your Organization: Propose a “Good Regulatory Practices” working group to drive continuous improvement.
By taking these steps, you can help raise the bar for regulatory compliance and public safety in our healthcare ecosystem.
Conclusion
The “Good Regulatory Practices in the Regulation of Medical Products” course offers a unique opportunity to learn directly from leading regulatory authorities and global experts. Whether you’re charting your first steps in DRA or seeking to refine your professional skill set, this module delivers actionable insights and practical tools—completely free of charge. Don’t miss out on this chance to elevate your regulatory knowledge and contribute to a more robust and transparent medical product oversight system.
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I am a rural practice owner and also a student of RMP(IA). I want to develop myself and skills. So I am interest with your courses.
As a practioner this course help me to develop personality, skill and career.
This looks like an essential course for any professional in the medical products landscape. A strong grasp of Good Regulatory Practices is the cornerstone of public trust and efficient market access. Highlighting this training is a great service to the industry, empowering professionals to uphold the highest standards of quality and safety. Highly valuable