Medical Device Regulations - FAQs Session with CDSCO
Voluntary Registration Process rolled out by CDSCO for Non Notified Devices is coming to an end  by Sep 30th 2021. Industry Forums are receiving so many FAQs from various stakeholders over the last 2 months asking many questions on Voluntary Regn Process and raising wide range of questions on WHAT HAPPENS FROM OCTOBER 1ST 2021.

Hence AIMED (Association of Indian Medical Device Industry) is organising a session to enable the industry, stakeholders to get their FAQs addressed from the Regulator.

Some of the FAQs raised by stakeholders are captured below and we invite industry, stakeholders to register and join the session to discuss pertinent issues , challenges faced, if any.  

This program is the initiative of AIMED , a leading Industry Platform for Make in India Manufacturers representing the Voice of the Industry.


Program Details :

Date - Sep 19th 2021, Sunday

Time - 4 PM - 5 PM

Mode - Online Meeting / Discussion


Program is Open for all Industry Members, Stakeholders like Manufacturers, Traders, Distributors, Startups, Med Tech Businesses etc.

There is NO REGISTRATION FEE but Prior Registration is a MUST.

Registered Participants shall get Email Confirmation 2 days before the session.

Contact Coordinates :

Ms Rama Venugopal
Email - contact@ccc-consultants.org 
WhatsApp - +919840870532

Mr D Srikanthan
Email - secretariat@ccc-consultants.org 
WhatsApp - +9003056539

Program Brochure and Details - http://ccc-consultants.org/medical-device-regulations/

Please fill up the delegate registration form listed below to receive program confirmation mail.

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