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EMA - Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 February 2022

10th March 2022

Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 February 2022

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EMA - PRIME enables earlier availability of life-changing medicines

10th March 2022

EMA’s PRIority Medicines (PRIME) scheme has had a positive impact on the authorisation of new medicines.

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FDA - New bill seeks to revamp FDA’s accelerated approvals programme

10th March 2022

New bill seeks to revamp FDA’s accelerated approvals programme

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Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 15-16 February 2022

10th March 2022

Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 15-16 February 2022

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MHRA - MHRA Good Practice Symposia Week (7 to 11 March 2022)

2nd March 2022

MHRA Good Practice Symposia Week (7 to 11 March 2022)

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MHRA - Regulators’ experience of clinical trials during the Covid-19 pandemic (Part 3) – looking forward

2nd March 2022

Blog Post - Regulators’ experience of clinical trials during the Covid-19 pandemic (Part 3) – looking forward

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MHRA - March Board Meeting and January Minutes

24th February 2022

The next MHRA Board Meeting held in public will be conducted virtually by webinar on Tuesday, 15 March 2022 from 10.00 until 12.30 hrs. (GMT).

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MHRA - Q1 2022 Events

24th February 2022

There are currently 5 separate events planned for March 2022.

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EMA - key recommendations in 2021 on the authorisation and safety monitoring of medicines for human use.

16th February 2022

EMA has published an overview of its key recommendations in 2021 on the authorisation and safety monitoring of medicines for human use.

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EMA - CTIS Bitesize Talks

15th February 2022

In 2022, EMA will offer short talks for clinical trial sponsors focused on CTIS functionalities.

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