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Katharina Friedrich
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Leader background:
Katharina Friedrich is a medical writing consultant with experience in MDR regulatory writing. She is based in Heidelberg, Germany and works as a Freelance Medical Writing Consultant with focus on orthopedic and cardiovascular devices. She prepares Clinical Evaluation Plans and Reports, PMCF Plans and Reports and SSCPs in compliance with MDR 2017/745 for class I to class III devices. She also supports development projects and the conduction of PMCF activities. As medical doctor she has experience in the field of orthopedic and trauma surgery.
Workshops:
Post-market Clinical Follow-up for Medical Devices
    Level: Foundation Area: Medical Devices
    Code: MDF4 Duration: 03:30:00
Understanding Instructions for Use of Medical Devices and Providing Support in Their Drafting
    Level: Foundation Area: Medical Devices
    Code: MDF5 Duration: 03:30:00
How to Compile the Summary of Safety and Clinical Performance (SSCP) for Medical Devices VIRTUAL WORKSHOP
    Level: Foundation Area: Medical Devices
    Code: MDF7 Duration: 03:00:00
Writing the State for the Art of medical devices according to the EU Medical Devices Regulation
    Level: Foundation Area: Medical Devices
    Code: MDF9 Duration: 03:30:00