Process Validation & Innovation
Process validation helps you to improve quality and reduce risks in your manufacturing process. It ensures a successful manufacturing process that produces quality parts and minimizes unexpected issues. Samwell has been an expert in process validation and support our customers in achieving success with every project.
Process Validation
Samwell is proud to have ISO 13485 certification, which means that we have established and implemented a quality management system that meets the strict requirements of this internationally recognized standard. Our ISO 13485 certification shows our commitment to providing the highest quality manufacturing processes to the medical device industry.
Validation Four Steps
We are able to produce precise medical products that are compliant with this standard.
Design Qualification (DQ), Installation Qualification (IQ)
Operational Qualification (OQ), Performance Qualification (PQ)
Innovation
Samwell endorses culture for innovation and is committed to be a well-rounded Technology Service Provider. We apply the spirit of constant innovation and improvement to our product and our work.
