Manufacturers of machines and systems for applications in medical technology must comply with the national and international stipulations of the regulators. The development and approval conditions are strict and create clear guidelines for engineering.
In addition to standards-based quality audits, there is a need for documentation. Traceability must also be guaranteed. These prerequisites also affect the procurement of technical components.
Ideally, you work with a partner who is familiar with the sector-specific and regulatory conditions. Bachofen guarantees that the products and solutions for medical technology are compatible with the application-specific regulations and standards.
You have a contact person at Bachofen who understands your business and provides competent support for you in the procurement process, for both standard and custom-made products. You therefore receive technical support when selecting the optimal components for the automation of your medical device or its system.