WORKSHOP ON INDIAN MEDICAL DEVICE REGULATIONS

LEARNING OBJECTIVE

• Candidate will get the knowledge on new legal requirements of the Indian Medical Device Regulations (IMDR).
• Overview of the safe and efficient manufacture of medical devices in accordance with the Indian Medical Device Regulations (MDR).
• To understand the responsibilities and obligations as a manufacturer, importers, and distributers of medical devices.

COURSE AGENDA

• Contents and Fundamentals of the Indian Medical Device Regulation (IMDR)
• Classification of Medical Devices
• Basic Requirements
• Content Requirements for Technical Documentation
• Validity of Conformity Assessment and Certification, Transition Periods
• Requirements for Manufacturers, Importers, Distributors and Service Partners

TARGET AUDIENCE

• Medical device manufacturers
• Consultants 
• Regulatory Affairs Specialists
• Expert advisors in medical devices regulatory affairs
• Working biomedical engineers / medical device professionals
• Pursuing Students are also eligible

Fee: INR 3,540 including 18% GST

CANDIDATES WILL BE PROVIDED WITH IBSC CERTIFICATE

TRAINING DURATION: 2 DAYS (9th & 10th June 2023)

LOCATION: Faculty of Pharmacy, MS Ramaiah University of Applied Sciences, Bangalore 

FOR QUOTATION SEND EMAIL TO TRAININGS@AMTZ.IN

NOTE: Travel & accommodation by candidate, hotel /PG details will be shared to registered participants.

After Receiving Confirmation Plan Your Travel.
If Not Received Minimum Number the Program May Postpone.
For more information, please contact

Mr. Nitturi Naresh Kumar
Mobile: +91-8897330990 | +91-7075737284
WhatsApp Link: https://wa.me/918897330990
WhatsApp Link: https://wa.me/917075737284
trainings@amtz.in