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You are here: Pharmya > All news > Guidance for the Transition of clinical trials from the Clinical Trials Directive to the Clinical Trials Regulation
EU-Guidance-for-the-transition-of-clinical-trials-form-directive-to-regulation_19July2023-1Download
Ryan McArthur 31 July 2023 All news
  • ← Notice to sponsors of clinical trials on medicinal products including advanced therapy medicinal products – Volume II Clinical trial vigilance
  • Early access to medicinal products →

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

  • European regulation on clinical trials for medicinal products: The end of the transition period
  • The ANSM publishes its haemovigilance report for 2023
  • User’s booklet – ANSM
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