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You are here: Pharmya > All news > Regulation (EU) 2017/745 – Questions & Answers regarding clinical investigation
EU-Regulation-EU-2017-745-Questions-and-answers-regarding-clinical-investigation-December-2023Download
Ryan McArthur 21 December 2023 All news
  • ← Questions and answers on describing adverse events in the product information (summary of product characteristics (SPC) and package leaflet (PL))
  • Artificial intelligence workplan to guide use of AI in medicines regulation →

Pharmya – Pharmacovigilance

PHARMYA is a French based company, dedicated to providing Pharmacovigilance services. Its mission is to support the pharmaceutical industry, biotechnology companies, research centers and their service providers in their efforts to comply with international Pharmacovigilance regulations.

In partnership with the region

Contact

  • PHARMYA
  • 315 Av. Saint Sauveur du Pin
  • 34980 Saint Clément de Rivière (Montpellier), France
  • Phone: +33 411 93 21 10
  • Email: info@pharmya.com
  • Website: www.pharmya.com

News

  • A common EU approach to data transparency in medicine regulation
  • Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 25-28 November 2024
  • European regulation on clinical trials for medicinal products: The end of the transition period
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