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  • 1.  New Member

    Posted 07-Jun-2024 18:40

    Hello members, 

    My name is Krunal Upadhyay. I am a Postgraduate pharmacy student with more than 8 years of experience in sterile injectable manufacturing pharma plants, and I am now pursuing my PGD in Regulatory Affairs at Conestoga College (Canada). In my carrier, I have been part of core QC documentation and submission of different products with respect to QC data (Specification, stability protocol), handling of change control, CAPA, and deviation. Also I was SME for pharmacopoeial change evaluation for USP, BP, Ph.Eur monographs. Working with USFDA, Health Canada, and EU-approved plants, I have acquired a wealth of knowledge of GMP, Compliance, 21 CFR requirements, and QMS to deliver the best products to patients.

    With my diverse experience in QC and operational activities of site I have moved my professional journey towards Regulatory affairs, and I am delighted to join this wonderful community. The knowledge I am getting on a day-to-day basis is really useful, and I am happy to connect with the Regulatory experts of this community to further strengthen my knowledge of different submissions. 



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    Krunal Upadhyay Pharm
    Postgraduate diploma Regulatory affairs student
    Sun Pharmaceutical industries limited
    Kitchener ON
    Canada
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