Admission

BEST PRACTICES IN MEDICAL DEVICE QUALITY AND REGULATORY

Date: 30-01-2024
BEST PRACTICES IN MEDICAL DEVICE QUALITY AND REGULATORY

The Biomedical Engineering Department successfully conducted a highly informative Faculty Development Program (FDP) on January 30, 2024, focusing on "Best Practices in Medical Device Quality and Regulatory." Attended by S4 and S6 students, the session featured Ms. Honey Thomas, an esteemed Associate Scientific Writer, as the resource person. Ms. Thomas shared invaluable insights into current medical device regulations and best practices for ensuring quality. The interactive discussion allowed students to engage directly with the expert, fostering a deeper understanding of the critical role of quality and regulatory compliance in the biomedical field. The event was a resounding success, providing students with practical knowledge and enhancing their awareness of industry standards.