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WHO publishes Variations Guideline for Prequalified APIs and Medicinal Products

https://seetharamkandarpa.webnode.in/news/who-publishes-variations-guideline-for-prequalified-apis-and-medicinal-products/

New EMA Inspection Requirements on Good Distribution Practices (GDP)

https://seetharamkandarpa.webnode.in/news/new-ema-inspection-requirements-on-good-distribution-practices-gdp-/

Denying, Delaying, And Refusing: How to Fail a FDA Inspection

https://seetharamkandarpa.webnode.in/news/denying-delaying-and-refusing-how-to-fail-a-fda-inspection/

New EMA Guideline on Starting Materials from Biological Medicinal Products

https://seetharamkandarpa.webnode.in/news/new-ema-guideline-on-starting-materials-from-biological-medicinal-products/

EMA Guideline on the use of bovine serum in the manufacture of human biological medicinal products

https://seetharamkandarpa.webnode.in/news/ema-guideline-on-the-use-of-bovine-serum-in-the-manufacture-of-human-biological-medicinal-products/

Black Triangle: a New EU Requirement

https://seetharamkandarpa.webnode.in/news/black-triangle-a-new-eu-requirement/

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