The information helps interested patient and consumer representatives to understand:
- the work of EMA;
- the types of activities patients and consumers are involved in.
Training overview
EMA has published a training overview describing the activities and materials available to patients and consumers taking part in EMA activities and events. This overview takes into account feedback obtained from patient and consumer organisations:
- CHMP early contact with patient and healthcare professional organisations: process and FAQs
- Training overview for patients and consumers involved in European Medicines Agency activities
- Involvement of patients in Scientific Advisory Group and Ad Hoc Expert meetings at EMA
- Involvement of patients in scientific advice procedures at the European Medicines Agency
Training Resources
EMA has developed a series of training videos targeted at patients and consumers entitled 'EMA basics'.
Together with the videos, EMA provides the presentation slides and related documents.
In-house training sessions
EMA holds an annual one-day training session for patients and consumers involved in EMA activities. The session offers an overview of medicines evaluation, with specific emphasis on when and how to get involved. Using a hands-on, interactive approach, participants learn about how they can contribute to scientific advice procedures, scientific-advisory-group meetings and reviewing information for patients.
For further information on annual training sessions, see:
- 2022 training session for patients, consumers and healthcare professionals (17-18/10/2022, 20/10/2022)
- 2021 training session for patients, consumers and healthcare professionals (24/11/2021)
- 2020 training session for patients, consumers and healthcare professionals (23/10/2020)
- 2017 training session for patients, consumers and healthcare professionals (21/11/2017)
- 2016 training session for patients and consumers (29/11/2016)
- 2015 training session for patients and consumers (25/11/2015)
- 2014 training session for patients and consumers (25/11/2014)
The video recording of the 2014 annual training session is available:
Workshops
For information on recent EMA workshops of particular relevance to patients and consumers, or where they have participated as speakers, see:
- Meeting of the CTTI/FDA Patient Engagement Collaborative (PEC) and EMA Patients and Consumers Working Party (PCWP)(01/07/2021)
- Workshop on the application of the General Data Protection Regulation (GDPR) in the area of health and Secondary Use of Data for Medicines and Public Health Purposes(23/09/2020)
- Workshop on benefit-risk of medicines used during pregnancy and breastfeeding(22/09/2020)
- ICH E6(R3) good clinical practice workshop with Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties(03/06/2020)
Webinars
Webinar on the Collaborare project, 4 April 2024
Webinar on transparency rules for the EU Clinical Trials Information System CTIS, 13 September 2023
Webinar on revision of the pharmaceutical legislation, 16 June 2023
CHMP early contact of patient and HCP organisations - training webinar, 19 April 2023
Information session on advanced therapy medicinal products (ATMPs) with PCWP and HCPWP on 28 June 2022
External training initiatives
Members of EMA's eligible organisation also have training initiatives that promote a better understanding of the development and approval of medicines as well as the involvement of patients and consumers in these processes. While EMA takes care in selecting external websites, it accepts no responsibility for the content.
European Patients Academy
The European Patients' Academy (EUPATI) is a public-private and multi-stakeholder partnership. It gathers patient organisations, academia and pharmaceutical industry.
EUPATI is an independent, non-profit foundation providing training and information on medicines research and development to patients and their representatives.
The Innovative Medicines Initiative (IMI) implemented EUPATI in 2012.
Open Academy School on Medicines Research and Development
The Open Academy School on Medicines Research and Development helps prepare patients to advocate for medicines development add equal access to treatments across Europe.
It ensures that medical information is clear, accurate and comprehensible.
EURORDIS-Rare Diseases Europe launched this training programme for patient experts in 2008.
European Patient Ambassador Programme
The European Patient Ambassador Programme (EPAP) is a self-learning programme. It introduces patients and carers to the essential skills and knowledge they need to interact with healthcare professionals, policy-makers, researchers and journalists.
The training programme was developed by the European Lung Foundation and the UK National Institute for Health Research Collaboration for Leadership in Applied Health Research and Care for Leeds, York and Bradford, with the help of patients, and professionals with expertise in key areas.