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EU-GMP: New Annex 16 released

https://seetharamkandarpa.webnode.in/news/eu-gmp-new-annex-16-released/

Who should review Batch Record?

https://seetharamkandarpa.webnode.in/news/who-should-review-batch-record-/

Revised Annex 16: Comments of the European QP Association

https://seetharamkandarpa.webnode.in/news/revised-annex-16-comments-of-the-european-qp-association/

European QP Association initiated a database comprising shared audits information

https://seetharamkandarpa.webnode.in/news/european-qp-association-initiated-a-database-comprising-shared-audits-information/

European QP Association: New Q&As published

https://seetharamkandarpa.webnode.in/news/european-qp-association-new-q-as-published/

Guidelines on requirements and expectations for the qualified person in a pharmaceutical company by DHMA

https://seetharamkandarpa.webnode.in/news/guidelines-on-requirements-and-expectations-for-the-qualified-person-in-a-pharmaceutical-company-by-dhma/

Final QP Declaration Template by EMA

https://seetharamkandarpa.webnode.in/news/final-qp-declaration-template-by-ema/

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