Table of Content 1. Evaluation activities for human medicines... 2

Similar documents
The European regulatory system for medicines and the European Medicines Agency

Work plan for GMP/GDP Inspectors Working Group for 2016

EU Clinical Trials Register. An agency of the European Union

Strategy and pilot phase for patient registries

List of nationally authorised medicinal products

The Clinical Trials Regulation EU No 536/2014: and Phase I trials

Reflection paper on non-spontaneous adverse event reports (peer-reviewed literature, internet and social media)

Quick Response (QR) codes in the labelling and package leaflet of centrally authorised 1 medicinal products

End of consultation (deadline for comments) 14 October Adoption by Committee for advanced therapies 15 October 2010

Clinical trials submitted in marketing-authorisation applications to the European Medicines Agency

The EU Clinical Trial Regulation A regulator s perspective

Enabling Discovery, Development, and translation of treatments for Cognitive Dysfunctions in Depression: A Workshop Session IV

EDQM Certificates of Suitability: Cooperation Among Inspectorates in Europe And Beyond

The EU portal and database

Questions & answers on signal management

1. Name of pharmacopoeia

Fluoride and Dental Health in Europe

Achieving Global Cyber Security Through Collaboration

Harmonizing Change Control Processes Globally

PROJECT: EURO-AUDITS THE EUROPEAN ROAD SAFETY AUDITOR TRAINING SYLLABUS APPENDIX E SURVEY RESULTS. October 2007

Standard operating procedure

Mutual recognition between the EU member states: official framework for collaboration saves resources?

EU PAS Register Guide

COMMITTEE FOR MEDICINAL PRODUCTS FOR HUMAN USE (CHMP)

Adoption by GCP Inspectors Working Group for consultation 14 June End of consultation (deadline for comments) 15 February 2012

ERASMUS+ MASTER LOANS

Implementation strategy for ISO IDMP in EU

NEW PASSENGER CAR REGISTRATIONS BY ALTERNATIVE FUEL TYPE IN THE EUROPEAN UNION 1 Quarter

Equity Release Schemes in the European Union

1. Perception of the Bancruptcy System Perception of In-court Reorganisation... 4

EMA Update Clinical Trials

Clinical trials in developing countries submitted to EMEA for regulatory purposes

The structure of the European education systems. schematic diagrams. Eurydice Highlights. Education and Training

EudraVigilance stakeholder change management plan

THE ORGANISATION AND FINANCING OF HEALTH CARE SYSTEM IN LATVIA

ERASMUS+ MASTER LOANS

European Surveillance of Veterinary Antimicrobial Consumption (ESVAC):

Finance information for postgraduate students

The structure of the European education systems 2012/13: schematic diagrams

INNOBAROMETER THE INNOVATION TRENDS AT EU ENTERPRISES

Reflection paper on the Use of Interactive Response Technologies (Interactive Voice/Web Response Systems) in Clinical Trials

The education system and lifelong learning in Finland. October 2015 Petri Haltia

Report from the CMDh meeting held on September !!! 3 months to go until the mandatory use of the electronic application form!!!

European Federation of Pharmaceutical Industries and Associations (EFPIA) HCP/HCO Disclosure Transparency Requirements Methodology Note for Shire

Project PESSIS 2 Title: Social Dialogue in the Social Services Sector in Europe

Introduction. Fields marked with * are mandatory.

Standard operating procedure

European Medicines Agency (EMA) Master Data Management Roadmap Substance, Product, Organisation and Referential data

Submission of comments on 'Policy 0070 on publication and access to clinical-trial data'

Reflection paper on clinical aspects related to tissue engineered products

An enabling volunteering infrastructure in Europe: Situation Trends Outlook

Pan-European opinion poll on occupational safety and health

ICH guideline Q10 on pharmaceutical quality system

Katy Taylor, European Coalition to End Animal Experiments (ECEAE), London, UK

Planned Healthcare in Europe for Lothian residents

SURVEY ON THE TRAINING OF GENERAL CARE NURSES IN THE EUROPEAN UNION. The current minimum training requirements for general care nurses

Association of the Councils of State and Supreme Administrative Jurisdictions of the EU

Operational Companies VAT Indirect Taxes. Why Luxembourg: VAT advantages for commercial companies*

Building up Specialized Cybercrime Units and Responsibilities for Managers. Virgil SPIRIDON ROMANIAN NATIONAL POLICE Head of National Cybercrime Unit

Energy prices in the EU Household electricity prices in the EU rose by 2.9% in 2014 Gas prices up by 2.0% in the EU

Contract Work in Switzerland. A Brief Guide

The Structure of the European Education Systems 2014/15:

TOWARDS PUBLIC PROCUREMENT KEY PERFORMANCE INDICATORS. Paulo Magina Public Sector Integrity Division

Good practice of dissemination and exploitation results in Latvia

Size and Development of the Shadow Economy of 31 European and 5 other OECD Countries from 2003 to 2015: Different Developments

ECRIN General Presentation

The Global Connector. European Connected Health Alliance. Test beds in European Ecosystems Brian O Connor, Chair, ECHAlliance

Finland must take a leap towards new innovations

Where science & ethics meet. The EFGCP Report on The Procedure for the Ethical Review of Protocols for Clinical Research Projects in Europe and Beyond

European judicial training Justice

ERASMUS+ MASTER LOANS

Alcohol Consumption in Ireland A Report for the Health Service Executive

Annex I. Article 31 of Directive 2001/83/EC. Procedure number: EMEA/H/A-31/1448

EMA esignature capabilities: frequently asked questions relating to practical and technical aspects of the implementation

QUEST improving the quality of urban mobility policies

Opinion/ Commission. Notification. Decision. Issued 2 / affected 3 amended on. 30/07/2015 Annex II, Labelling and PL

CENTRAL BANK OF CYPRUS

10TH EDITION MERGER CONTROL VADEMECUM FILING THRESHOLDS AND CLEARANCE CONDITIONS IN THE 29 EUROPEAN JURISDICTIONS

The European Commission s strategy on Corporate Social Responsibility (CSR) : achievements, shortcomings and future challenges

The Act imposes foreign exchange restrictions, i.e. performance of certain actions requires a relevant foreign exchange permit.

PLANT PROTECTION AND BIOCIDAL PRODUCT AUTHORISATION IN EUROPE

Standard operating procedure

Delegation in human resource management

INTERNATIONAL TRACKED POSTAGE SERVICE

Higher education institutions as places to integrate individual lifelong learning strategies

Waste. Copenhagen, 3 rd September Almut Reichel Project Manager Sustainable consumption and production & waste, European Environment Agency

Computing our Future Computer programming and coding in schools in Europe. Anja Balanskat, Senior Manager European Schoolnet

TPI: Traffic Psychology International on a common European curriculum for postgraduate education in traffic psychology

Compilation of Community Procedures on Inspections and Exchange of Information

FP7 Space Research Proposal evaluation and role of the REA European Commission REA S2 Space Research

Labour Force Survey 2014 Almost 10 million part-time workers in the EU would have preferred to work more Two-thirds were women

Michael Thomson BEDA President and Director, Design Connect, London

REPORT FROM THE COMMISSION TO THE EUROPEAN PARLIAMENT AND THE COUNCIL

2 ND CALL FOR PROPOSALS 27 October January 2009

Compilation of individual product-specific guidance on demonstration of bioequivalence

ERASMUS FOR YOUNG ENTREPRENEURS : A NEW EXCHANGE PROGRAMME

Wealth Accounting and Valuation of Ecosystem Services (WAVES): a Global Partnership. Natural Capital Accounting for Sustainable Development

Content & Aims Silke Weiß

Transcription:

20 February 2015 EMA/CAT/611200/2014 Procedure Management & Business Support Division 2015-2016 Table of Content 1. Evaluation activities for human medicines... 2 1.1. Pre-authorisation activities... 2 1.2. Initial-evaluation activities... 3 1.3. Other specialised areas and activities... 4 2. Horizontal activities and other areas... 5 2.1. Partners and stakeholders... 5 30 Churchill Place Canary Wharf London E14 5EU United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 Send a question via our website www.ema.europa.eu/contact An agency of the European Union European Medicines Agency, 2015. Reproduction is authorised provided the source is acknowledged.

1. Evaluation activities for human medicines 1.1. Pre-authorisation activities CAT aims to help National Competent Authorities (NCA) to build up their expertise on Advanced Therapy Medicinal Products (ATMPs) and awareness of ATMP related procedures such as evaluation of marketing authorisation applications, certification and classification. Some NCAs have reported problems when having to decide if a product would fulfil the criteria of an ATMP (e.g. in the framework of a clinical trial application). To support NCAs, CAT plans to provide training to the NCA on the criteria to apply for the classification of ATMPs. The training will be based on the experience gained by CAT with classification of ATMPs over the last 5 years, as reflected in the CAT Reflection Paper on classification. To set up a 2/3 hour webinar-training session for staff from NCAs / NCA innovation offices involved in classification questions for ATMPs. The aim of this training is to increase harmonisation of the classification outcomes throughout the EU. Identify and agree date and time for the webinar. Prepare the content of the training programme and adoption by CAT. Hold the training / webinar. 100% completion by end of 4 Q 2015 EMA topic leader: P Celis ; CAT topic leader: N Ferry Other Committee participants: E Flory, M Timon Member N Ferry France Alternate E Flory Germany Alternate M Timon Spain EMA/CAT/611200/2014 Page 2/5

1.2. Initial-evaluation activities Assessors in the NCA play an essential role in the evaluation of marketing authorisation applications for ATMPs, either directly when they are part of the Rapporteur or CoRapporteur teams, or indirectly when commenting upon the Rapporteur or CoRapporteur Assessment reports. Not so many ATMPs have been reviewed in the centralised system, so the experience build in the NCA might not be extensive. CAT therefore wants to assist the NCA to build up their expertise in the field and plans therefore to organise an assessor training session open to all NCAs. The training will be based on the experience gained by CAT. Depending on the topic of the training, the assessor training can also be opened to GMP and GCP inspectors in the member states. To develop and hold an assessor training for the evaluation of applications for marketing authorisation and certification of ATMPs. Identify the topic(s) of the assessor training Identify and agree date and time for the training. Ensure incorporation of the CAT assessor training in the EMA Network training initiative Activities in 2016 Hold the assessor training 100% completion by end of 2 Q 2016 EMA topic leader: P Celis ; CAT topic leader: M Menezes-Ferreira Other Committee participants: Paula Salmikangas, Martina Schüßler-Lenz, Simona Badoi Alternate Margarida Menezes- Portugal Ferreira Member Martina Schüßler-Menz Germany Member Simona Badoi Romania EMA/CAT/611200/2014 Page 3/5

1.3. Other specialised areas and activities Understand trends in R&D of ATMPs via the analysis of EudraCT for the years 2010 to 2014. To extract information from EudraCT for the years 2010-2014 using the same filters as used for the analysis for the years 2004-2010 on: the profile of sponsor of clinical trials with ATMPs, the products under development, the indications investigated, etc. Compare the results with outcome of the EudraCT analysis for 2004-2010. Analyse and compare the profile of ATMP developers and the ATMPs under development with that in non-eu regions/countries (e.g. USA, Canada). Extract the raw data from EudraCT with the help of the EMA colleagues in charge of the EudraCT database: by end of 1 Q 2015 Data cleaning, e.g. to remove duplicate entries (e.g. multi-country trials) and trials not related to ATMPs: by end of 2 Q 2015 Analysis of data: by end of 3 Q 2015 Report to CAT and prepare a publication: by end of 4 Q 2015 EMA topic leader: P Celis ; CAT topic leader: Ilona Reisch Other Committee participants: P Salmikangas, N Ferry, R Maciulaitis, M Menezes-Ferreira, D Sladowski, E French, M Lipucci, B Gänsbacher, T Boráň Member Ilona Reisch Austria Member Nicolas Ferry France Member Romaldas Maciulaitis Lithuania Member Dariusz Sladowski Poland Member Elaine French UK Member Michele Lipucci Patients Organisation Member Bernd Gänsbacher Doctors Organisation Alternate Margarida Menezes- Portugal Ferreira Member Tomáš Boráň Czech Republic EMA/CAT/611200/2014 Page 4/5

2. Horizontal activities and other areas 2.1. Partners and stakeholders Provide assistance to ATMP developers via the organisation of a scientific workshop in collaboration with a scientific society. One of the long-term objective of the CAT is to strengthen dialogue with stakeholders and provide tutorial training and workshops for ATMP developers. Such workshop took place in 2011, 2013 and 2014. In 2015, CAT plans to organise a fourth CAT workshop with a scientific society. On basis of contact with learned societies, a partner for a joint workshop will be selected not later than the beginning of 2015. A programme Committee with representative of the CAT, the scientific society and the EMA will be set up to develop the programme and to identify the presenters / speakers. The draft programme will be presented to the CAT in the 2 Q 2015. The CAT workshop will be held in the 2 nd half of 2015. EMA topic leader: P Celis ; CAT topic leader: Paula Salmikangas Other Committee participants: Dariusz Sladowski, Tiina Palomäki, Martina Schüßler-Lenz Member Dariusz Sladowski Poland Member Tiina Palomäki Finland Member Martina Schüßler-Lenz Germany EMA/CAT/611200/2014 Page 5/5