Florian Krafft leads Consulting Services at Johner Institut GmbH, specializing in guiding medical device manufacturers through complex international regulations like MDR, IVDR, and FDA approval. A graduate of Technische Universität Berlin, his background includes roles in product management and as a Person Responsible for Regulatory Compliance (PRRC).
He actively engages with the digital health community, participating in major European trade fairs such as MEDICA in Düsseldorf and DMEA in Berlin. Florian is passionate about supporting innovators and start-ups in the MedTech space, helping them navigate the path to product approval and market launch.
Unique Fact: He positions regulatory affairs professionals as the "real heroes" who help companies overcome significant hurdles in the industry.
Read the full overview →Behavioral traits and communication patterns that shape how this person evaluates opportunities, builds trust, and makes decisions in professional settings.
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