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Pharmaceuticals and Medical Devices Agency (PDMA) - Japan


Know about Good Manufacturing Practice guidelines provided by Pharmaceuticals and Medical Devices Agency (PDMA) - Japan.
Pharmaceuticals and Medical Devices Agency (PMDA) was formed in April 1, 2004 to provide the cGMP pharmaceutical guideline to the nation. Relief services for adverse health effects, GMP inspection of drug manufacturing facilities and post marketing safety measures are the main services of PMDA.

Good Manufacturing Practice Updates


Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips.
Email: .moc.enilediugamrahp@ofni Need Help: Ask Question


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