Medical Devices Testing

Following the Medical device regulation EU 2017/745, evaluating medical devices is a crucial aspect of ensuring their safety, efficacy, and compliance with regulatory standards before they can be declared as safe to use. Conducting the biological evaluation plan, biocompatibility testing, chemical characterization testing, and toxicological risk assessment will be the finest approach for the successful mitigation of biological risks and, therefore, the assurance of the medical device’s safety.

 

Why QACS, The Challenge Test Lab

At QACS we offer GLP compliant, ISO 9001 and ISO 17025 accredited laboratory testing services to support clients with what Medical Device Regulation mandates, which will enable you to:

• evaluate your medical device and its components
• minimize the cost and time for designing, producing and marketing of the product
• develop your product with regulatory compliance
• provide a safe and efficient product

For Medical Device testing contact us –  [email protected] – +30 210 29 34745