08 Apr Date April 8, 2025 Author Akshaya The Role of Indian Authorized Agent in Medical Device Industry The medical device industry in India has undergone significant transformation and growth over the past few years. This growth is p...
08 Nov Date November 8, 2024 Author Akshaya The Fourth and Fifth Schedule Audits The Fourth and Fifth Schedule Audits, conducted by either a Notified Body or the Central Licensing Authority (CLA), are essential...
22 Sep Date September 22, 2024 Author Akshaya Class C and D notified medical device manufacturing registration in India CDSCO - The Government Authority Medical device registration in India is overseen by the Central Drugs Standard Control Organisati...
06 Aug Date August 6, 2024 Author Akshaya What is Endorsement in the Context of Medical Device Licensing in India In the Indian medical device regulatory landscape governed by the Central Drugs Standard Control Organization (CDSCO), an "endorse...
30 Jul Date July 30, 2024 Author Akshaya Here are some of the common mistakes that can occur during the submission of a medical device manufacturing license application in India Incomplete or Inaccurate Information: Missing Documents: Not including all the required documents as per the CDSCO guidelines...
25 May Date May 25, 2024 Author Akshaya Class A non-sterile non-measuring medical devices registration in India Class A non-sterile non-measuring medical devices - Final notification GSR 777(E) was released by the Indian Ministry of Health an...
20 Mar Date March 20, 2024 Author Akshaya Medical Device Regulation in India By 2025, the rapidly expanding Indian healthcare sector will generate $280 billion in revenue. One of the top 20 medical device ma...