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 > EMA releases practical guidance for procedures related to Brexit for centralised products

EMA releases practical guidance for procedures related to Brexit for centralised products
Document

admin 6 March 2019 All news
  • ← We are certified according to ISO 9001:2015
  • Pharmya attends the Joint MEB/DIA Excellence in Pharmacovigilance training →

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

  • New product information wording – Extracts from Pharmacovigilance Risk Assessment Committee (PRAC) recommendations on signals
  • List of European Union reference dates and frequency of submission of periodic safety update reports
  • Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 20-23 July 2020
Copyright © 2018 - Pharmya - Legal terms - Quality Policy