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New Requirements of the FDA on Stability Testing of Generic Drugs

https://seetharamkandarpa.webnode.in/news/new-requirements-of-the-fda-on-stability-testing-of-generic-drugs/

Draft Guideline ICH Q3D for Elemental Impurities published!

https://seetharamkandarpa.webnode.in/news/draft-guideline-ich-q3d-for-elemental-impurities-published-/

ICH reviews future ICH topics and its Organisation

https://seetharamkandarpa.webnode.in/news/ich-reviews-future-ich-topics-and-its-organisation/

New presentation on "Future Activities of ICH from the FDA Point of View"

https://seetharamkandarpa.webnode.in/news/new-presentation-on-future-activities-of-ich-from-the-fda-point-of-view/

New Process Validation Guideline by EMA

https://seetharamkandarpa.webnode.in/news/new-process-validation-guideline-by-ema/

Elemental impurities: ICH Q3D has reached step 4 (final guideline)

https://seetharamkandarpa.webnode.in/news/elemental-impurities-ich-q3d-has-reached-step-4-final-guideline-/

Training Presentation on 'ICH Q10: Pharmaceutical Quality System'

https://seetharamkandarpa.webnode.in/news/training-presentation-on-ich-q10-pharmaceutical-quality-system/

Training Presentation on 'ICH Q9: Quality Risk Management'

https://seetharamkandarpa.webnode.in/news/training-presentation-on-ich-q9-quality-risk-management/

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