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