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You are here: Pharmya > All news > MHRA – Send and receive information on adverse drug reactions (ADRs)

https://www.gov.uk/guidance/send-and-receive-information-on-adverse-drug-reactions-adrs

Philippe Calandra 4 January 2021 All news
  • ← CMDh Q&A – Pharmacovigilance Legislation
  • MHRA – Periodic Safety Update Reports (PSURs) for 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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