News Archive

EMA - Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 March 2022

22nd March 2022

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 March 2022

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MHRA - Delivering High Standards in Medicines Advertising Regulation 2021 Annual Report

22nd March 2022

Delivering High Standards in Medicines Advertising Regulation, 2021 Annual Report

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MHRA Webinar - Medicines Supply to Northern Ireland

22nd March 2022

MHRA Webinar: Medicines Supply to Northern Ireland

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MRC announces plans to halve carbon footprint by 2030

22nd March 2022

MRC announces plans to halve carbon footprint by 2030, 14th March 2022

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Safety Observer - RSI in Clinical Trials: MHRA Findings and Tips

22nd March 2022

Safety Observer Article - RSI in Clinical Trials: MHRA Findings and Tips

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UKRI - Shared commitment to improve public involvement in research

22nd March 2022

UK Research and Innovation (UKRI) has signed a shared commitment to improve public involvement in health and social care research.

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MHRA Blog - Compliance Monitor process (Part 1) – An introduction

16th March 2022

Compliance Monitor process (Part 1) – An introduction

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EC - Political and legal issues linked to financing the development of pharmaceuticals all along their life-cycle

10th March 2022

Presentations and recording - HPP webinar: “Political and legal issues linked to financing the development of pharmaceuticals all along their life-cycle” (03 March 2021)

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EMA - Regulation on EMA’s extended mandate becomes applicable

10th March 2022

The regulation reinforcing EMA’s role in crisis preparedness and management of medicinal products and medical devices becomes applicable as of 1st March 2022. It puts some of the structures and processes established by EMA during the COVID-19 pandemic on a more permanent footing, while entrusting several new tasks to the Agency.

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EMA - Highlights of 2021

10th March 2022

Human and Veterinary Highlights from 2021

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