European Medicines Agency (EMA) Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties meeting with all eligible organisations

• Date:
  Tiistai, 15 marraskuu 2022, Koko päivä
• Paikka:
  Online
  European Medicines Agency, Amsterdam, the Netherlands

This meeting brings together all eligible patient and consumer and healthcare professionals organisations and members of the Patients' and Consumers' Working Party (PCWP) and Healthcare Professionals' Working Party (HCPWP).

The meeting focuses on the following topics:

• Patient involvement in medicines development and regulation including feedback from Patient Experience Data workshop and CIOMS report
• Update from Task Force on availability of authorised medicines
• Health Technology Assessment – interconnection of regulatory and HTA activities and role of patients and HCP
• Future activities on antimicrobial resistance.

Video recordings

Report from EMA Multistakeholder Workshop on Patient Experience Data - Rosa Gonzalez-Quevedo (EMA)

 

CIOMS report on ‘Patient involvement in the development, regulation and safe use of medicines’ - François Houÿez (EURORDIS) & Lembit Rägo (CIOMS)

 

Update on the TF AAM activities - Monica Dias (EMA) & Hugues Malonne (HMA)

 

Reporting of shortages by organisations - Inga Abed (EMA)

 

Preparation for multistakeholder workshop in 2023 - Monica Dias (EMA)

 

Update on EU guidance on shortage prevention and communication to the public - Inga Abed (EMA)

 

Implementation of Regulation (EU) 2021/2282 on Health Technology Assessment - Valentina Barbuto (EC)

 

“Sequential decision making”: how regulatory and HTA activities interconnect under the new HTA Regulation - Michael Berntgen (EMA)

 

The delivery under the EMA/EUnetHTA 21 work plan: focus on engagement with patients and HCPs - regulatory and HTA activities interconnect under the new HTA Regulation
3:50:00 – 4:10:31 Stephanie

 

Lessons learnt from COVID - 19 Melanie Carr (EMA)

 

Preparation for multistakeholder workshop on AMR in 2023 - Radu Botgros (EMA) & Ivana Silva (EMA)

Documents

Agenda - PCWP/HCPWP annual meeting with all eligible organisations - 15 November 2022

Draft Reference Number: EMA/605514/2022

Meeting summary - PCWP/HCPWP annual meeting with all eligible organisations - 15 November 2022

Reference Number: EMA/775191/2021

Presentation - Implementation of Regulation (EU) 20212282 on Health Technology Assessment - C Barbuto (EC)

Presentation - ”Sequential decision making” how regulatory and HTA activities interconnect under the new HTA Regulation - M Berntgen (EMA)

Presentation - CIOMS report on ‘Patient involvement in the development, regulation and safe use of medicines’ - F Houÿez (EURORDIS)

Presentation - CIOMS report on ‘Patient involvement in the development, regulation and safe use of medicines’ - L Rägo (CIOMS)

Presentation - Lessons learnt from COVID-19 - M Carr (EMA)

Presentation - Preparation for multistakeholder workshop in 2023 - M Dias (EMA)

Presentation - Preparation for multistakeholder workshop on AMR in 2023 - R Botgros (EMA)

Presentation - Report from EMA Multistakeholder Workshop on Patient Experience Data - R Gonzalez-Quevedo (EMA)

Presentation - Reporting of shortages by EU patient and healthcare professional organisations - I Abed (EMA)

Presentation - The delivery under the EMA/EUnetHTA 21 work plan focus on engagement with patients and HCPs - S. Said and A. Willemsen (EunetHTA 21)

Presentation - Update of the HMA/EMA Task Force on availability of authorised medicines for human and veterinary use (TF AAM)- M Dias (EMA) and H Malonne (HMA)

Presentation - Update on EU guidance on shortage prevention and communication to the public - I Abed (EMA)

Presentation - Introduction to discussion topics on "Access to medicines"