EMA published the final version of the Data Quality Framework for EU medicines regulation
EMA’s new data quality framework for medicines regulation
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News
DARWIN EU®: open call for data partners
Expressions of interest to be considered as a candidate Data Partner for DARWIN EU® are open
3Rs testing approaches: EMA seeks feedback on guideline revision
Submission of comments on the Concept paper on the revision of the Guideline on the principles of regulatory acceptance of 3Rs (replacement, reduction, refinement) testing approaches is now open.
Tribute to Dr Torrent-Farnell, pioneer in the field of rare diseases
It is with great sadness we learnt of the passing of Dr Josep Torrent-Farnell on 1st December.
Annalisa Landi appointed steering group member of ENCePP
We are pleased to announce that Annalisa Landi has been just appointed as Steering Group member of the European Network of Centres for Pharmacoepidemiology and Pharmacovigilance for term 2024-2026.
Sickle Cell Disease: Lancet recommendations in Italy
The meeting “La Malattia Drepanocitica – nuove sfide e prospettive in Italia con le raccomandazioni della Commission di Lancet Haematology” will be held in Rome on 20 November 2023 at Sala Zuccari, Palazzo Giustiniani.
Dose rationale for gabapentin and tramadol in paediatric pain
Professor Adriana Ceci from Fondazione Gianni Benzi, cooperated as co-author to the article “Dose rationale for gabapentin and tramadol in pediatric patients with chronic pain” just published in the Pharmacology Research & Perspectives journal.
Technology transfer meets HTA and innovation procurement
CRO in Aviano and 6 italian partners will organise a two-day event on 11-17 October 2023, focused on Technology Transfer, Health Technology Assessment and Innovation Procurement
EMA seeks new data partners for RWE in DARWIN EU
The European Medicines Agency (EMA) is looking for new data partners to collaborate with DARWIN EU® – the Data Analysis and Real-World Interrogation Network.
EMA opens consultation on AI in medicines lifecycle
EMA published a draft reflection paper on the use of artificial intelligence to support the safe and effective development, regulation and use of human and veterinary medicines.
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