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Juni 27, 2022 - Juni 27, 2022 /

Clinical Suite | Clinical Evaluation under the MDR

CE Certification Klinische Bewertung Market Access Europe MDR 2017/745 Medical Device Regulations Training

Juni 30, 2022 - Juli 07, 2022 /

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

CE Approved CE Certification CE-Registrierung Market Access Europe MDR 2017/745 Medical Device Regulations PRRC Einhaltung gesetzlicher Vorschriften Training

Ergebnisse

Juni 27, 2022 - Juni 27, 2022 /

Clinical Suite | Clinical Evaluation under the MDR

CE Certification Klinische Bewertung Market Access Europe MDR 2017/745 Medical Device Regulations Training

Juni 30, 2022 - Juli 07, 2022 /

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

CE Approved CE Certification CE-Registrierung Market Access Europe MDR 2017/745 Medical Device Regulations PRRC Einhaltung gesetzlicher Vorschriften Training

Juni 30, 2022 - Juni 30, 2022 / Virtual

Clinical Suite | Literature Search Design for Medical Devices

CE-Registrierung CER Klinische Angelegenheiten Medical Device Regulations Training Literature search Medical Devices

Juli 26, 2022 - Juli 26, 2022 /

Free Webinar | UK market access: UKCA challenges in uncertain times

UK Responsible Person UKCA

September 11, 2022 - September 13, 2022 / USA

Meet and Greet with Qserve Experts at RAPS Convergence 2022

Konferenz In-Vitro-Diagnostik Medical Device Regulations RAPS

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