Expert Talk on Regulatory Guidelines in Medical Devices
April 6, 2026 2026-04-07 9:14Expert Talk on Regulatory Guidelines in Medical Devices
Expert Talk on Regulatory Guidelines in Medical Devices
Name of Department: Faculty of Pharmacy
Venue: Mahapragya Hall
Event Coordinator: Ms. Isha
Date of Event: 06-04-26
Time: 10:00 A.M. onwards

Organized by: Placebo Club, School of Pharmacy, S. Lal Singh Memorial College of Pharmacy and Mata Jarnail Kaur College of Pharmacy, Desh Bhagat University, Mandi Gobindgarh, Punjab, in collaboration with the Institution’s Innovation Council (IIC) and Internal Quality Assurance Cell (IQAC).

The Faculty of Pharmacy, Desh Bhagat University, organized an Expert Talk on Regulatory Guidelines in Medical Devices on 6th April 2026 with great enthusiasm. The session was delivered by Mr. Gaurav Kapila, U.S. Head, Regulatory Affairs (Lab Instruments and Software Chapter), Roche Diagnostics, Indianapolis, USA. The event was conducted virtually, enabling wide participation and smooth interaction.
Objectives of the Program
The primary objective of the session was to provide participants with comprehensive insights into global regulatory frameworks governing medical devices. The speaker elaborated on key regulatory pathways, compliance requirements, and documentation processes essential for medical device approval in international markets such as U.S. and Europe. The talk also focused on enhancing students’ understanding of regulatory affairs as a career domain, highlighting current industry practices, emerging trends, and required skill sets. Real-world examples and case studies were discussed to bridge the gap between theoretical knowledge and practical application.

The event witnessed enthusiastic participation from B. Pharmacy students, along with faculty members. Students actively engaged in the session and participated in the interactive Q&A segment, gaining valuable clarity on regulatory guidelines and career opportunities in this field.
Overall, the expert talk was highly informative and beneficial, enriching the knowledge of participants and providing them with a broader perspective on the importance of regulatory compliance in the medical device industry.
Outcomes of the Event
- Participants gained comprehensive knowledge about global regulatory frameworks governing medical devices, including approval pathways and compliance standards.
- The session enhanced understanding of regulatory requirements, documentation, and quality assurance practices essential in the medical device industry.
- Students and faculty were introduced to current industry trends and real-world challenges in regulatory affairs.
- The talk provided valuable insights into career opportunities in regulatory affairs, motivating students to explore this field.
- Interaction during the Q&A session helped clarify practical doubts and encouraged active participation and critical thinking.
- The event strengthened academic-industry collaboration, bridging the gap between theoretical knowledge and practical application.

Vote of Thanks
Dr. Puja Gulatu, Director, School of Pharmacy delivered the Vote of Thanks. She expressed her sincere gratitude to the esteemed speaker, Gaurav Kapila, for sharing his valuable time, knowledge, and industry expertise with the participants.. She appreciated his insightful presentation, which greatly enriched the understanding of regulatory guidelines in medical devices. She also extended thanks to the organizing committee, including the School of Pharmacy and collaborating bodies (IIC & IQAC), for successfully arranging the event, faculty members and students for their enthusiastic participation and engagement and IT team for ensuring the smooth execution of the virtual session. She concluded by acknowledging everyone’s contribution in making the event a grand success. Ms. Khushpal Kaur, Principal, Mata Jarnail K College of Pharmacy and Dr. Shailash Kumar was also there.
Conclusion
The expert talk on “Regulatory Guidelines in Medical Devices” was a highly successful and enriching session. It provided participants with a deeper understanding of regulatory processes, compliance requirements, and industry expectations in the field of medical devices. The session not only enhanced academic knowledge but also inspired students to consider career pathways in regulatory affairs and healthcare industries. Overall, the event served as a valuable platform for knowledge exchange, professional development, and strengthening industry-academia connections.