WHAT IS IT ABOUT?
C1 | Commercialization: How do I generate revenue in the healthcare industry?
C2 | Certification: How do I get my product and company certified?
C3 | Clinical Studies: How can I provide the necessary evidence by collecting clinical data?
C4 | Copyright: How can I leverage data and intellectual property rights to my advantage?
4C Business Modelling®: How are the 4Cs connected and how do I integrate them into a business model that is entrepreneurially successful AND regulatory compliant?
WHAT IS THE GOAL?
- You will have identified corresponding barriers to shorten the time-to-market and considered them in an individual project plan.
- You will be familiar with the reimbursement options in the healthcare market(e.g., self-payer, AMNOG or selective contracts).
- You will know how quality management systems (e.g.,ISO 13485, Good manufacturing practice (GMP)) and regulatory processes become a strategic concept and how they effectively lead to approval of your product (e.g.,Medical Device Regulation, In-Vitro-Diagnostic Regulation, Medicinal Products Act).
- You will be able to assess whether and what kind of clinical studies you need and how to best implement them(e.g., ISO 14155, ICH Guidelines).
- You will know how to deal with data protection requirements (DSGVO) and how to strategically protect and exploit intellectual propertyrights(e.g., patent).
More information can be found on the official website of the program: https://mi-incubator.com/en/4c-accelerator/
Deadline to apply for the next round is 7th July 2025