Ashutosh Mishra

Sr. Manager-Mindray Medical India Pvt. Ltd

Role
Sr Manager Regulatory Affairs at Mindray India
Location
Gurugram, HR, IN
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Ashutosh Mishra

Application for Grant for manufacturing license & Loan License (MD-03, MD-04,MD-07 & MD-08) of Class A, B, C&D as per Medical Device Rules-2017 online Portal.Import license MD-14 of medical devices and component. Prepare technical file, Risk analysis report, Clinical evaluation report (MEDEV 2.7.2 Rev 04), Post market Surveillance (MEDEV 1.12/1 ), PMCF (MEDEV 2.12/2) Prepare Device Master File (DMF) & Essential Principles Checklist as per Medical Device Rules-2017. Prepare Site Master File as per Medical Device Rules-2017. Audit faced for the renewal of ISO-13485:2016 certification.Ensure to maintain Quality Management system as per standard/guidelines requirements, GDP, ISO 9001, ISO 13485;2016, FDA- QSR 21 CFR Part 820, European MDR, 21 CFR Part 803 (Medical Device reporting).For post-market changes, ensure impact assessment is identified in the affected country and change notifications are submitted accordingly with minimum impact on product supply.

Experience

  1. Sr Manager Regulatory Affairs

    Mindray India

    Feb 2026 — Present

Education

  • U P Technical University

    M. Pharmacy, Pharmacy

    2008 — 2011

  • UP Technical Board

    B.Pharmacy, Science

    1999 — 2001

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Ashutosh Mishra — Sr Manager Regulatory Affairs at Mindray India in Gurugram, HR, IN | Unifers