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Author Archives: Akshaya

Medfins International > Articles by: Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya
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...
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0 Comments Author Akshaya

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  • The Role of Indian Authorized Agent in Medical Device IndustryApril 8, 2025
  • Case Study 1: U.S. Endotracheal Tube Manufacturer – Achieving 21 CFR 820 Compliance & 510(k) Submission with Medfins International.February 13, 2025
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