Skip to content
MEDICRO
  • Clinical research
    • Study planning
    • Regulatory Affairs
    • Project management
    • Monitoring
    • Quality Management
    • Data management / Statistics
    • Medical Writing
    • (Pharmaco-)Vigilance
    • Clinical evaluation
  • Trials in Europe
    • Regulatory Consulting (human drug studies)
    • Regulatory Consulting (medical devices)
    • Study Start-up
    • Monitoring
    • Project Management
    • Medical Writing
    • Project Rescue
  • Translations
    • Medical Texts
    • Clinical Research
    • Medical Technology
    • Legal Texts and General Translations
    • Certified Translations
    • Proofreading
    • Localization
    • Languages
    • Expertise
  • About us
    • CRO
    • Translation Department
    • Blog
    • Publications
    • Downloads
    • Career
    • Contact
  • Glossary

Month: February 2019

19. February 2019 No comment(s)

Reporting Incidents and Serious Adverse Events (SAEs) During the Use of Medical Devices in Germany

Recording, reporting and evaluating side effects during clinical trials on drugs and after the drugs’ marketing authorisation is imperative for the safety of patients. With medical devices, too, patient safety has priority. Unlike with drugs, though, the safety of users and third parties is also recorded here. This article shall highlight the differences between an…

  • MEDICRO GmbH • Klostersteig 19 • D-91580 Petersaurach
  •  +49 9872 9699027
  • +49 9872 9699029
  • office@medicro.de
             
  • Contact
  • Legal Notice
  • Privacy Policy
  • T&C
© MEDICRO 2023
This website uses cookies. If you continue to use the website, we will assume your consent.OKPrivacy policy