Symposium 2024

HM1: Ensuring regulatory excellence

2024-11-08T06:51:00+00:00By Sandra Lourenço

HM2: European clinical research ecosystem – How to boost its competitiveness

2024-11-08T06:51:00+00:00By Natasha Bankowski

HM3: Regulation and innovation – Keeping up with the times (Fireside chat)

2024-11-08T06:51:00+00:00By Céline Combet

HM4: Electronic product information (ePI) – A digital passport for medicinal product information

2024-11-08T06:51:00+00:00By Sarah Heraghty

HM5/MD1/IVD1: COMBINE project: A new era of combined clinical trials in Europe

2024-11-08T06:52:00+00:00By Erica Cypas and Charlotte Holleran

HM6: Artificial Intelligence – How will AI and machine learning tools transform regulatory practice?

2024-11-08T06:52:00+00:00By Natasha Bankowski

HM7: Clinical evidence generation in Europe – Is it time for a more holistic view of global healthcare product development?

2024-11-08T06:52:00+00:00By Michelle Blake

HM8: How the new EU regulation on health technology assessment (HTA) will change clinical drug development and regulatory affairs

2024-11-08T06:53:00+00:00By David Uguen

HM9: Clinical trial applications - EU Clinical Trial Regulation and beyond

2024-11-08T06:53:00+00:00By Christine Grew

PS1: Resolving specific development hurdles via scientific advice

2024-11-08T06:55:00+00:00By Ophélie Poujade

Leaders:

PS2: Patient experience data – The next steps towards medicines evaluation

2024-11-08T06:56:00+00:00By Anna Koptina

SME: Regulatory updates for SME, academia and start-ups

2024-11-08T06:55:00+00:00By Marie Uguen

MD2/IVD2: Unravelling AI as a medical device - Insights into the EU AI Act and other global perspectives

2024-11-08T06:56:00+00:00By Margareth Jorvid

MD3/IVD3: The impact of MDR/IVDR and its effect on future developments of policies, manufacturers and inspectorates

2024-11-08T06:56:00+00:00By Maïté Barthel

MD4/IVD4: UK MDR – Current requirements and future perspectives for medical devices and in vitro diagnostics

2024-11-08T06:56:00+00:00By Mehryar Behizad

MD5/IVD5: Responsible and experienced PRRCs for MDR and IVDR

2024-11-08T06:57:00+00:00By Rachel Drapela

VM1: Advancing regulatory policies for One Health – A holistic approach to animal and public health

2024-11-08T06:57:00+00:00By Kornelia Grein

VM2: Progress in veterinary regulatory procedures – Opportunities and threats concerning the implementation of Regulation (EU) 2019/6

2024-11-08T06:57:00+00:00By Rick Clayton

VM3: Navigating the regulatory landscape of veterinary product information

2024-11-08T06:57:00+00:00By Catarina Ferreira

VM4: Advancing veterinary pharmacovigilance – Insights into signal management, first experiences with PhV inspections and introducing the EMA-ADR Data Quality Framework

2024-11-08T06:58:00+00:00By Kornelia Grein