Q&A ETH - CAS Regulatory Thinking
In an interactive Q&A we introduce the program and the organisers. In pharma, medicine and the medtech industry, human beings play the central role. Even if one rightfully thinks of the patient first and the attending physician second in this context, these stakeholders do not yet represent all interest groups that have a legitimate concern for healthcare products.
CAS RT is aimed at (non-)experts in the healthcare business who want to learn why it is important to know about development processes, validation instruments, alternatives in clinical trials and different certification and reimbursement strategies for medtech, pharma, (digital) biomarkers, in-vitro diagnostics, software or AI as medical device. Participants will become generalists that are highly needed in the changing healthcare sector: Whether you're a start-up or business leader looking to drive a business forward, a government employee looking to ensure the safety of healthcare products, a payer looking to reimburse healthcare expenses, or defining new reimbursement paths – Regulatory Thinking will teach you how to participate successfully in the healthcare business.
Date: 8th November
Time: 17:00 – 17:45
Location: Online