Design Control & Validation
The group works with identifying user needs — including clinical requirements —turning them into design input requirements, developing the matching design output specifications, and securing comprehensive design verification and validation to confirm that the finished device meets those needs.
Guidelines for Expert Groups
As part of being a member of Medicoindustrien, it is possible to participate in our expert groups. These groups are open to all employees of member companies who possess expert knowledge or have a professional interest in the group’s area of work.
- Each expert group appoints a chairperson from among its members
- The chairperson prepares the meeting agenda in collaboration with Medicoindustrien’s secretariat
- Expert groups hold 2–4 meetings per year
- Meetings are held at Medicoindustrien’s offices or hosted by members companies
- Meetings are subject to internal confidentiality
- Members confirm or decline meeting participation via the website
