Validation
Ensuring compliance with the highest safety standards
Medical device manufacturers are required to adhere to strict guidelines when it comes to validating their equipment and processes. At DesignPro Automation, we have a dedicated team of experts who support the creation of clear, accessible technical documentation for the design, test and build of our advanced automated solutions. Our engineers have successfully integrated systems into highly regulated environments such as; ISO Class 8 production.
All machines come with an extensive list of documentation
- Operation Manual
- Bills of Materials
- Mechanical Drawings
- Electrical Drawings
- CE Certification
- Pneumatics Drawings
- Standard Parts Info
- Functional Design Specification (FDS)
- Software Design Specification (SDS)
- Product Contact Material Report
Featured Projects
Explore our most recent work
Laser Marking Solution Powers Medical Device Innovation
Project Overview A leading global medical device manufacturer partnered with DesignPro Automation to develop a precise, efficient laser marking solution for their R&D department ...
Boosting Medical Device Production with Automated Inspection & Packaging
Enhancing Medical Device Production through Automated Inspection and Packaging Solutions INDUSTRY: Medical Device CLIENT: A Global Leader In Plastic Injection Molding Overview DesignPro was ...
Automated Cartoning System
Automation technologies can help simplify the most complex packaging operation, saving installation time, cutting costs and minimising floorspace. In this project our client, one ...