Dr. Heike Fischer is Director Clinical Research. She has been advising multinational MedTech companies on strategic clinical and regulatory planning with the aim of accelerating market entry and generating sustainable growth. Her focus is on partnering with start-up to large-size companies optimize product development, master regulatory requirements, support reimbursement strategies and develop targeted and efficient clinical investigation plans. This includes hands-on support in implementing a (digital) QMH (ISO 13485) creating technical documentation / design dossier and conducting global clinical investigations.