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You are here: Pharmya > All news > Guidance on the handling of applications for Centrally Authorised Products (CAPs) pending on 1 January 2021

This guidance sets out how the MHRA will handle centralised applications that are still pending on 1 January 2021.

Philippe Calandra 14 September 2020 All news
  • ← Registration of clinical trials for investigational medicinal products and publication of summary results from 1 January 2021
  • Regulating medical devices from 1 January 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.

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

  • A common EU approach to data transparency in medicine regulation
  • 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
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