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Written Confirmation: A Questions & Answer Document of the Danish Authority provides further Clarifications

https://seetharamkandarpa.webnode.in/news/written-confirmation-a-questions-answer-document-of-the-danish-authority-provides-further-clarifications/

Frequently asked GMP question: How should active substance auditors be qualified?

https://seetharamkandarpa.webnode.in/news/frequently-asked-gmp-question-how-should-active-substance-auditors-be-qualified-/

Authorisation of Generic Drugs in the USA: Requirements on APIs Stability Data for US Drug Master Files

https://seetharamkandarpa.webnode.in/news/authorisation-of-generic-drugs-in-the-usa-requirements-on-apis-stability-data-for-us-drug-master-files/

Stability Testing of Generics: FDA publishes Q&A Document

https://seetharamkandarpa.webnode.in/news/stability-testing-of-generics-fda-publishes-q-a-document/

USP visual inspection expert answers for question regarding AQL testing

https://seetharamkandarpa.webnode.in/news/usp-visual-inspection-expert-answers-for-question-regarding-aql-testing/

My new Mobile Application "SRK GMP FAQ"

https://seetharamkandarpa.webnode.in/news/test/

Question & Answer Document on GDP by European Commission

https://seetharamkandarpa.webnode.in/news/question-answer-document-on-gdp-by-european-commission-/

MHRA's Interpretation of Cross Contamination & PDEs

https://seetharamkandarpa.webnode.in/news/mhras-interpretation-of-cross-contamination-pdes/

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