Pharmya

  • Home
  • About us
  • Services
    • Pharmacovigilance Systems
    • Operational Pharmacovigilance Activities
    • EU QPPV & Local QPPV services
    • Pharmacovigilance Audits and Training
  • News
  • Careers
  • Contact us
  • English
  • Français
  • Español
You are here: Pharmya > All news > European Medicines Agency post-authorisation procedural advice for users of the centralised procedure

https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/european-medicines-agency-post-authorisation-procedural-advice-users-centralised-procedure_en.pdf

Philippe Calandra 13 September 2021 All news
  • ← Risk Minimisation Activities (RMA) – Belgium
  • Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 13-16 September 2021 →

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.

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

  • China : release of MedDRA Coding Guidance for Adverse DrugReaction (ADR) Reports
  • Medical literature and the entry of relevant information into the EudraVigilance database by the European Medicines Agency
  • Questions and Answers Regarding the Implementation of a Risk-Prioritized Periodic Safety Update Report Regulatory Review Pilot (PSUR-RRP) at Health Canada
Copyright © 2018 - Pharmya - Legal terms - Quality Policy