Webinar on Regulations for Medical Devices
AIMED (Association of Indian Medical Device Industry) is organising a webinar session for the benefit of MSME Manufacturers in the Medical Device Manufacturing space , to guide them about the Registration Process to be completed with the Regulators as per MDR 17. This is an exclusive session for Manufacturers who are into manufacture of Category A and B Products (both Sterile and Non Sterile Products). The session will cover wide range of topics , as listed below, which shall be addressed by Industry Members, Regulators, Experts :
- Fast Tracking of Registration Process for Class A & B Non Sterile and Sterile Product Manufacturers
- Submission of Forms Online, Payment Process etc for Online Registration
- FAQs by MSME Manufacturers – an overview
- ISO 13485 Certification – What did the Regulator Prescribe ?
- Clean Room Guidelines – What needs to be addressed by Manufacturers ?
Program Details :
Date – April 9th 2022, Saturday
Time – 3:00 PM to 05:30 PM
There is NO REGISTRATION FEE. This is an Industry Awareness Session – designed for the Industry, by the Industry Association.
Registration Link is shared below :
For detailed information about Webinar, download the Program Brochure by clicking the button below :
This program is hosted by IIT Kanpur SIIC (Startup Incubation and Innovation Centre, IIT Kanpur)
Request you all to register for this session and circulate the information to industry and other key stakeholders.