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You are here: Pharmya > All news > NOTICE TO CLINICAL TRIALS PROMOTERS OF MEDICINAL PRODUCTS INCLUDING INNOVATIVE THERAPY MEDICINAL PRODUCTS

Volume II. Vigilance of clinical trials Conduct of research involving the human person mentioned in 1 ° of Article L. 1121-1 of the public health code relating to the drug: Adverse reaction reporting, developments and reports annual security JANUARY 2020

admin 12 February 2020 All news
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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

  • The European Medicines Agency (EMA) is delivering a Product Management Service (PMS) and a Substance Management Service (SMS) to support regulatory activities in the European Union (EU)
  • Drug clinical trials: the CTIS portal becomes the sole entry point for new requests as of the 31st of January 2023
  • Work Plan 2023 of the Pharmacovigilance Risk Assessment Committee (PRAC)
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