MedTech

Reliability is essential when serving the high-tech medical industries. Process control via traceability, tailor-made fixed process lines, PPAP on component evaluation, state-gate approvals and numerous other requirements must be fulfilled to serve you in accordance with the serious needs in MedTech.

Traceability and certification are key

It is a given that all regulatory must be respected and an underlying certification in ISO 13485 is the process guide to cover this in the most advanced methodical way. Thinking and arranging a supply network and enabling the reliable handling of the same is a crucial element of success. This goes from manufacturability studies over NPI to a reliable series manufacturing and obsolescence management.

GPV offers full traceability in the electronic manufacturing phase and in risk management in the development phase, and our electronics sites in Denmark, Switzerland, Austria, Thailand, and Mexico are all certified according to the medical standard ISO 13485.

Your value-adding EMS partner

This uncompromising approach to regulative demands and industry best-practice standards within MedTech allows our customers to focus on their core business while we serve as a value-adding outsourcing EMS partner with full commitment and project ownership.

Our product solutions and services within electronic manufacturing for the medical industry include:

BUSINESS CASE

Laboratory Equipment

Leading life science company that develops laboratory equipment, consumables, and services used in research, pharmaceutical, and laboratories worldwide.

GPV produces PCBAs and semi box-build, operating within a high-mix, low-volume setup that aligns well with the customer’s footprint. Our R&D team is well positioned to support future product development.