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You are here: Pharmya > All news > EMA – Clinical Trials Information System (CTIS)

https://www.ema.europa.eu/en/human-regulatory/research-development/clinical-trials/clinical-trial-regulation

Philippe Calandra 22 March 2021 All news
  • ← EMA Management Board – highlights of March 2021 meeting
  • Reporting of serious adverse events and effects, new facts with or without urgent safety measures, and Annual Safety Report →

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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