(EU) 2023/607, 26th May 2024 deadline approaching

The Future of Health Grant welcomes confinis as a new Program Partner

Transitioning to the Medical Device Regulation (MDR) 2017/745

Deadline for transitioning to the Medical Device Regulation

A Step Forward in Medical Device Manufacturing: the New QMSR Aligned with ISO 13485:2016

The EU Artificial Intelligence Act and Medical Device Regulation with Andrea Biasiucci

Leveraging Real-World Evidence: Insights and Guidance for Medical Device Manufacturers

confinis ag appoints Dario Motti as lead of new Digital Health Competence Cluster

Change in Management Structure with Appointment of New CEO at confinis ag

The Medical Device Regulation and the medical care for children and rare diseases

Working at confinis and the IVDR world with Barbara Jeroncic

IVD News – IVDR Date of Application, new Guidance Documents

confinis and deep tech with Andrea Biasiucci

Electromagnetic Compatibility (EMC) of Medical Devices

IVD News – Progressive Roll-Out and MDCG 2022-2 on Clinical Evidence

UK Responsible Person Services

confinis launches new UK Responsible Person service in UK

ISO/FDIS 11608 series opened for voting

confinis partners with Irdeto to launch the first cybersecurity assessment tool in the medical devices industry

confinis offers Swiss Representative Service

Exporting Swiss Medical Devices to the EU

Join our Startup Workshop 2021!

How does the notified body assess your clinical evaluation?

How to perform a clinical evaluation for Medical Device Software

How to ensure sufficient clinical evidence for legacy devices

How to claim an equivalence in the clinical evaluation under the MDR

Bei Medizinprodukten auf die EU warten hilft der Schweiz wenig