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You are here: Pharmya > All news > Hong Kong – Guidance for Pharmaceutical Industry – Adverse Drug Reaction Reporting Requirements
Hong-Kong-Guidance_for-Pharmaceutical_Industry_ADR-reporting-requirements-V1_01Aug2021-1Télécharger
Philippe Calandra 23 August 2021 All news
  • ← Reporting of local drug related safety report, progress report and final study report in clinical trial – Hong Kong
  • Switzerland – Guidance for Industry electronic exchange of ICSRs through ElViS HMV4 →

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

  • 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
  • The ANSM publishes its haemovigilance report for 2023
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