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You are here: Pharmya > Articles by: Ryan McArthur
EMA – Risk management plans – Update
2023 October Oct 02

EMA – Risk management plans – Update

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Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 25-28 September 2023
2023 September Sep 29

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 25-28 September 2023

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European contact points for clinical trials
2023 September Sep 25

European contact points for clinical trials

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Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 11-14 September 2023
2023 September Sep 21

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 11-14 September 2023

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Clinical Trials Regulation (EU) No 536/2014 in practice
2023 September Sep 18

Clinical Trials Regulation (EU) No 536/2014 in practice

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Committee for medicinal products for human use (CHMP) – Minutes for the meeting on 19-22 June 2023
2023 September Sep 14

Committee for medicinal products for human use (CHMP) – Minutes for the meeting on 19-22 June 2023

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United Kingdom – Pharmacovigilance Inspection Metrics Report April 2021 – March 2022
2023 September Sep 11

United Kingdom – Pharmacovigilance Inspection Metrics Report April 2021 – March 2022

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Innovation in medicines
2023 September Sep 08

Innovation in medicines

https://www.ema.europa.eu/en/human-regulatory/research-development/innovation-medicines#itf-briefing-meetings–section

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Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 28-31 August 2023
2023 September Sep 04

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 28-31 August 2023

https://www.ema.europa.eu/en/news/meeting-highlights-pharmacovigilance-risk-assessment-committee-prac-28-31-august-2023

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Minutes of PRAC meeting on 10-12 May 2023
2023 September Sep 01

Minutes of PRAC meeting on 10-12 May 2023

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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.

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

  • Pharmacovigilance Risk Assessment Committee (PRAC) – Minutes of PRAC meeting on 13 – 16 January 2025
  • CTIS newsflash – 25 March 2025
  • 2024 Annual Report on EudraVigilance for the European Parliament, the Council and the Commission
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