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You are here: Pharmya > All news > Questions and answers – Clinical Trials Information System (CTIS) and Clinical Trials Regulation (CTR)
EU-questions-answers-query-management-working-group-ctis-ctr_Feb2023-1Download
Ryan McArthur 3 March 2023 All news
  • ← List of medicines under additional monitoring
  • Letter to QPPVs – International Transfer of ICSRs from EV and GDPR →

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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