Thursday 26th of May 2022 is a significant day for those operating with in vitro diagnostic (IVD) medical devices in the European Union (EU). This is the date of application...
Product development and usability engineering of medical devices, risk management and patient safety, regulatory requirements and quality management systems are Clinipower’s core competences.
- Are you thinking of developing a product or software?
- Is your organization planning to take a leap into health technology?
- Do you recognize the need to change your organization’s operational culture?
- Do you need more information about the impact of regulatory changes on your business?
We have the answers. We are offering our experience, knowledge and skills for your benefit – plus the spirit of making things happen that is our hallmark.
Contact us, and let’s figure out together where to start!