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ICH

by sdran | | OUS-Regulatory: Other National Reg. Agencies & international Res.

The International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) is a unique project that brings together the regulatory authorities of Europe, Japan and the United States and experts from the...

Japan Ministry of Health, Labor and Welfare

by sdran | | OUS-Regulatory: Other National Reg. Agencies & international Res.

VISIT SITE

EU Comission

by sdran | | OUS-Regulatory: Other National Reg. Agencies & international Res.

VISIT SITE

MHRA

by sdran | | OUS-Regulatory: Other National Reg. Agencies & international Res.

The MHRA is an executive agency of the Department of Health of UK which is responsible for ensuring that medicines and medical devices work, and are acceptably safe. VISIT SITE

EMA

by sdran | | OUS-Regulatory: Other National Reg. Agencies & international Res.

European Medicines Agency (EMA) is a decentralized body of the European Union with headquarters in London. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary...
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Recent Posts

  • AMDM Fall Focus Meeting
  • 2025 Member Appreciation Event
  • SDRAN/RAPS RAC Drug and Device Exam Practice Questions Workshop
  • How to Prepare for a Regulatory Inspection: Planning for Success
  • Artificial Intelligence Meets Regulation: EU AI Act, MDR and IVDR in Practice

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