The 1st International Conference on Rare Diseases and Paediatric Research, organized by EPTRI, was a virtual event held on November 18-19, 2021.
1st conference on rare diseases and paediatric research on-demand
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ICH-GCP Training Course for Clinical Research Professionals
CVBF is pleased to present its e-learning “ICH-Good Clinical Practice (GCP) Training Course” a guide for professionals involved in clinical research
M&S Workshop for Rare Diseases Research Methodologies
A face-to-face workshop entitled “Modelling & Simulation: Research Methodologies for Small Populations in Rare Diseases” organised in the context of EJP RD’s ERN Workshop
Rare diseases clinical trials toolbox: a practical guide
The Rare Diseases Clinical Trials Toolbox has been developed as a practical aid for developers of clinical trials on medicinal products for human use regardless of therapeutic area.
ERN research training workshops: apply by 25 April
The ERN Research Training Workshops funding opportunity is now open for applications until April 25th.
EMA reports 5-year impact of PRIME scheme on drug approval
A report presenting the results from the first five years of the EMA PRIority Medicines (PRIME) scheme, has just been published.
Italy’s Law 175: support for Rare Diseases and Orphan Medicines
Law no. 175 of 10 November 2021, including the provisions for the treatment of rare diseases and for the support of the research and development of orphan medicinal products, has been approved. It officially entered into force in December 2021.
HTA of paediatric medicines: challenges and opportunities
The article Health technology assessment of paediatric medicines: European landscape, challenges and opportunities inside the conect4children project has been recently published in the British Journal of Clinical Pharmacology.
Overview of EU PAS Register Studies: 2010-2018
The article “Overview of the EU PAS register post-authorization studies performed in Europe from September 2010 to December 2018” has been recently published in the Pharmacoepidemiology & Drug Safety journal. The study provides a detailed description of all...
EDPB guidelines on right of access open for consultation
The EDPB has just published its Guidelines 01/2022 on data subject rights-Right of access open for public consultation until March 11th, 2022
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