We are ISO 29993:2017 Certified
MDD to MDR Implementation
- Date: 7th and 8th May 2022
- Time: 5:30pm to 9:00pm
- Fees: Rs.10000+1180 (GST)=11800/-
Learning Objective:
- Need for Comprehensive Regulation of Medical Devices
- Medical Device Rules 2017
- Difference between MDR against MDD
- Importance of MDR and all definitions
- Regulatory requirements for registration of Medical devices in Europe and USFDA 510(k), PMS routes
- Regulatory requirements for registration of Medical devices in India, SUGAM portal submission and its Challenges
Who can attend??
Pharma & Medical Device Industry Professionals, Biomedical Engineers, Consultants, Regulatory Professionals, Student and who are willing to make career MEDICAL DEVICE industry.
Mode:
Zoom Meeting link shared via Email and WhatsApp Requirements: Laptop, iPad or Android Phone with Good Internet Connection
For further enquiry, kindly contact on: 9819125208/9821144706
Email us at:rajahsrio@gmail.com, services@raajgprac.com, raajgprac@gmail.com OR Visit our website: www.raajpharmaelearning.comTo register for the webinar, please click on: https://lnkd.in/g43Q5TE4