The Committee for Advanced Therapies (CAT) is the European Medicines Agency's (EMA) committee responsible for assessing the quality, safety and efficacy of advanced therapy medicinal products (ATMPs) and following scientific developments in the field.
It was established in accordance with Regulation (EC) No 1394/2007 on ATMPs as a multidisciplinary committee, gathering some of the best available experts in Europe.
Role of the CAT
The committee's main responsibility is to prepare a draft opinion on each ATMP application submitted to EMA, before the Committee for Medicinal Products for Human Use (CHMP) adopts a final opinion on the marketing authorisation of the medicine concerned.
At the request of EMA's Executive Director or the European Commission, the CAT can also draw up an opinion on any scientific matter relating to ATMPs.
The CAT also:
- participates in certifying quality and non-clinical data for small and medium-sized enterprises developing ATMPs;
- participates in providing scientific recommendations on the classification of ATMPs;
- contributes to scientific advice, in cooperation with the Scientific Advice Working Party (SAWP);
- takes part in any procedure delivering advice on the conduct of efficacy follow-up, pharmacovigilance or risk-management systems for ATMPs;
- advises the CHMP on any medicinal product that may require expertise in ATMPs for the evaluation of its quality, safety or efficacy;
- assists scientifically in developing any documents relating to the objectives of the Regulation on ATMPs;
- provides scientific expertise and advice for any Community initiative related to the development of innovative medicines and therapies that requires expertise on ATMPs;
- supports the work programmes of the CHMP working parties.
The CAT's work plan includes developing guidance documents, contributing to cross-committee projects, work on simplification of procedures and requirements for ATMPs, training for assessors and organising scientific workshops.
The CAT held four workshops in cooperation with learned societies to strengthen dialogue with stakeholders and provide guidance for ATMP developers:
- Workshop with the European Society for Gene and Cell Therapy (27/10/2011);
- Workshop with the Translational Centre for Regenerative Medicine Leipzig (23/10/2013);
- Workshop with the German Society for Transfusion Medicine and Immunohematology and the German Stem Cell Network (11/09/14);
- Workshop with the International Society for Cellular Therapy (ISCT) in Seville (25/09/2015).
How useful is this page?
Average rating:Based on 3 ratings
Add your rating:
- See all ratings
1 ratings0 ratings0 ratings1 ratings1 ratings
European Medicines Agency
30 Churchill Place
London E14 5EU