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Independent Regulatory Affairs and Clinical Evaluation Expert at Germany
Florian Tolkmitt is a biomedical engineer with a background in Medical Device Development focused on single-use devices and implants. He has been in the Regulatory Affairs and Clinical Evaluation field for more than 10 years and has compiled his first Clinical Evaluation Report according to the first version of MEDDEV 2.7/1. Over the past years he has grown his network of medical writers and consultants and has founded PRO-LIANCE GLOBAL SOLUTIONS just recently in order to serve the Medical Device industry in all regards to Clinical Data Management and Regulatory Affairs.