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重点

九月 25, 2024 - 九月 26, 2024 /

Qserve Training | Understanding the AI Act: Implications for Medical Device and IVD Compliance

Join our 2-day training program in Amsterdam (The Netherlands), where we delve into the pivotal EU AI Act, a comprehensive horizontal legislation aimed at regulating AI across all member states.

AI In-Vitro Diagnostics Medical Device Regulations Medical Devices

九月 12, 2024 - 二月 13, 2025 /

Startup Training Suite

A training suite designed for medical device startups navigating the complex regulatory landscape.

In-Vitro Diagnostics Medical Devices Startups Training

结果

八月 20, 2024 - 八月 20, 2024 /

Clinical Suite | Clinical Evaluation

Clinical Affairs Clinical Evaluation Market Access Europe MDR 2017/745 Medical Device Regulations Training

八月 22, 2024 - 八月 29, 2024 /

Virtual Training | ISO 13485

九月 03, 2024 - 九月 10, 2024 /

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

CE Certification PRRC Regulatory Compliance

九月 04, 2024 - 九月 04, 2024 /

Free Webinar | Navigating the Regulatory Landscape for Innovative Biomedical Applications

Medical Device Regulations Medical Devices MedTech

九月 12, 2024 - 二月 13, 2025 /

Startup Training Suite

A training suite designed for medical device startups navigating the complex regulatory landscape.

In-Vitro Diagnostics Medical Devices Startups Training

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