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You are here: Pharmya > All news > Regulating medical devices in the UK

https://www.gov.uk/guidance/regulating-medical-devices-in-the-uk

Philippe Calandra 3 January 2022 All news
  • ← Instructions for Authorization Holders Related to Letters to Healthcare Professionals (DHPC)
  • Guidance on the electronic submission of information on investigational medicinal products for human use in the Extended EudraVigilance medicinal product dictionary (XEVMPD →

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

  • Clinical trials for medicines: apply for authorisation in the UK
  • Changes to the guidance document Temporary authorisation of human medicinal products HMV4
  • Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 10 – 13 January 2022
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