Regulatory Affairs Executive (Kundli)

Regulatory Affairs Executive (Kundli)

09 Sep
|
MACOM
|
Kundli

09 Sep

MACOM

Kundli

1. Preparation of documentation for submission to FDA for medical device approval and/or response to FDA inquiries
2. Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017.

📌 Regulatory Affairs Executive (Kundli)
🏢 MACOM
📍 Kundli

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