Anne-Sophie Grell
Manager Regulatory Affairs Medical Devices
20+ years experience in QA & RA for Medical Devices
Anne-Sophie brings over two decades of expertise in Quality Assurance and Regulatory Affairs for Medical Devices. As Manager of Regulatory Affairs, she leads our team in navigating complex regulatory landscapes and ensuring manufacturers achieve compliance with EU MDR, FDA, and international standards.
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Summary of Commission Implementing Regulation (EU) 2025/1234
Learn how Commission Implementing Regulation (EU) 2025/1234 broadens electronic Instructions for Use (eIFUs) for professional medical devices, the compliance steps required, and how IFUcare can help.
The Future of Post-Market Surveillance in IVD and MD Industry: Leveraging eIFU
Post-market surveillance has become more critical than ever. Learn how eIFU can revolutionize PMS in the IVD and MD industry.
IFUcare: Its History, Evolution of eIFU Regulations and the Road Ahead
IFUcare's journey since 2007 provides insight into how the IVD and MD world is evolving. Learn about the company's growth and the regulatory landscape.
Defining the Future of eIFU Services
A Q&A with Dimitri Jordens addressing how changing customer needs and evolving regulatory requirements are impacting eIFU innovations.
The IFUcare Touch: How a Commitment to Customer Support Spells Success
The right customer support is the hallmark of a valuable partner. Learn how Thermo Fisher Scientific benefits from IFUcare's decade-long partnership.
How an Orthopaedic Implant Start-up Benefited from eIFU Management
Since 2019, Bonebridge, a Swiss manufacturer of smart orthopaedic trauma implants, has partnered with IFUcare to develop eIFU for their products.