Political agreement on the draft EU Clinical Trials Regulation could enhance regulatory framework for clinical trials, but is not ambitious enough.

20.12.2013

20 December 2013, Brussels – EuropaBio welcomes the political agreementon the draft Clinical Trials Regulation by the EU Committee of Permanent Representatives (COREPER) today, thus paving the way for the adoption of the Regulation by the co-legislators, the European Parliament and the Council, in 2014.  The Clinical Trials Regulation however must reflect a balanced approach with regards to competitive assessment timelines and the disclosure of clinical trial data.

A quick adoption and considered implementation of the Regulation will contribute to achieving greater harmonisation and efficiency in the regulatory framework for clinical trials, whilst maintaining high standards of patient safety and robustness of clinical data.

Nevertheless, we believe that the compromise text agreed by Member States today is not ambitious enough to meet the objective of securing timely patient access to innovative treatments and improving the attractiveness of Europe in terms of clinical research, and thus contributing to the growth objective of the Europe 2020 Strategy.

 

Assessment timelines

According to the agreement backed by Member States today, national authorities would grant clinical trial approval at 60 days; however, the timeline could be extended by 50 days for advanced therapy medicinal products. EuropaBio fears that these extended timelines lack ambition and signal that there is little commitment to restoring a competitive environment for conducting clinical research in Europe.

Including the timelines for questions and assessment of responses, the total assessment timelines would actually be nearer to or in many cases exceeding 100 days.Noting that Member States such as Belgium and the UK have put in place shorter timelines of around 30 days, such aproposal would bring little or no improvement to the current situation in many European countries. At best, it would speed up approvals in countries that currently have longer timelines.

 

Access to clinical trials data

EuropaBio recognises the scientific and public interest in access to clinical trial data and supports measures to achieve this. We believe that a balanced approach on data transparency measures will support Europe’s attractiveness for clinical research; however, the measures agreed today raise a number of technical questions that will need to be addressed. 

Miriam Gargesi, Director of Healthcare at EuropaBio stated: “Whilst we welcome the revision of the Clinical Trials Directive as a commitment to stimulate clinical research in Europe, we are concerned that the proposal adopted today in the EU Committee of Permanent Representatives may not fully achieve the intended objective to provide a harmonised and efficient framework for clinical research in the EU. In particular, the Regulation should be carefully implemented so as not to jeopardise companies’ innovation potential and as patients’ timely access to innovative medicines.”

 

 

About EuropaBio

EuropaBio is the European Association for Bioindustries and was created in 1996. Our mission is to create an innovative and dynamic biotechnology-based industry in Europe.

Our membership is composed of 55 corporate members, 15 associate members and Bio regions, and 17 national biotechnology associations, who in turn represent more than 1800 small and medium sized biotech companies in Europe.

Members of EuropaBio are involved in research, development, testing, manufacturing and commercialisation of biotechnology products and processes. Our corporate members have a wide range of activities: human and animal health care, diagnostics, bio-informatics, chemicals, crop protection, agriculture, food and environmental products and services.

 

Contact:

Marie Blanchard

Healthcare Biotechnology Officer

EuropaBio

Email: m.blanchard@europabio.org

Ph: +32 (0) 2 739 11 74/ +32 (0) 477 33 42 91

 

 

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