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You are here: Pharmya > All news > Product Management Service (PMS) – Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe

https://www.ema.europa.eu/en/human-regulatory/research-development/data-medicines-iso-idmp-standards/spor-master-data/substance-product-data-management-services

Marie Berger 8 August 2022 All news
  • ← Covid-19 Vaccine Surveillance Update – Period 17-Jun-2022 to 21-Jul-2022
  • Switzerland : safety of medicines →

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 contact points for clinical trials
  • Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 11-14 September 2023
  • Clinical Trials Regulation (EU) No 536/2014 in practice
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