WORKSHOP ON INDIAN MEDICAL DEVICE REGULATIONS

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Workshop on Indian Medical Device Rules 2017 Indian Medical Device Regulations workshop ensures the safety and effectiveness of medical devices and gives overview of the efficient and safe manufacture of medical devices. LEARNING OBJECTIVE Candidate will get the knowledge on new legal… 

Notified Bodies registered with CDSCO under MDR 2017

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List of Notified Bodies registered with CDSCO under MDR 2017 CDSCO has released the list of Notified Bodies registered with CDSCO under Medical Devices Rules 2017 to carry out audit of manufacturing site under the provisions of said rules. Please… 

Frequently Asked Questions (FAQs) on Medical Device Rule, 2017

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CDSCO has released a document on Frequently Asked Questions on Medical Device Rule, 2017 Central Drugs Standard Control Organization (CDSCO) . Directorate General of Health Services, Ministry of Health and Family Welfare, has released a Document on FAQs on Medical… 

Medical Device Pathway in India

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Startup Incubation and Innovation Centre, IIT Kanpur for a brainstorming session- ‘Medical Device Pathway in India’ Startup Incubation and Innovation Centre, IIT Kanpur conducted a brainstorming session- ‘Medical Device Pathway in India’ along with two renowned dignitaries – Ms. Meena… 

CDSCO Notification

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Central Drugs Standard Control Organisation – Notification dated 11th July 2022 In pursuance of notification No. G.S.R. 102(E) dated 11.02.2020, all non-notified medical devices of Class A & Class B categories are scheduled to enter licensing regime with effect from…