All Symposium 2024 articles

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VM5: Exploring the future of veterinary regulatory affairs – Harnessing science and innovation for animal health excellence

2024-11-08T06:58:00Z

 

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

2024-11-08T06:58:00Z

 

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

2024-11-08T06:57:00Z

 

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VM3: Navigating the regulatory landscape of veterinary product information

2024-11-08T06:57:00Z

 

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

2024-11-08T06:57:00Z

 

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

2024-11-08T06:57:00Z

 

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

2024-11-08T06:56:00Z

 

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

2024-11-08T06:56:00Z

 

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

2024-11-08T06:56:00Z

 

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

2024-11-08T06:56:00Z

 

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TOPRA annual lecture: Status of global health

2024-11-08T06:55:00Z

 

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

2024-11-08T06:55:00Z

 

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PS1: Resolving specific development hurdles via scientific advice

2024-11-08T06:55:00Z

Regulatory Rapporteur November 2024 | Volume 21 | No.10 Leaders: Sandra Lourenço, Director of Regulatory Affairs, Arriello, Ireland Andrea Laslop, Head of Scientific Office, Austrian Agency for Health and Food Safety, Austria Speakers: Peggy Sarah, the ...

Journal

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

2024-11-08T06:53:00Z

 

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

2024-11-08T06:53:00Z

 

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

2024-11-08T06:52:00Z

 

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

2024-11-08T06:52:00Z

 

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

2024-11-08T06:52:00Z

 

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

2024-11-08T06:51:00Z

 

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

2024-11-08T06:51:00Z