Carmel Laboratories possess the technical proficiency, equipment and experience for the successful execution of medical device packaging, transportation, distribution cycles and environmental testing: handling, vehicle stacking, vibration, loose load vibration, temperature, humidity, altitude, accelerated aging, Etc.
The technical proficiency is complemented by RA and QA experts that provide the regulatory guidance and ensure compliance with the applicable medical device standards and regulation.
Carmel Laboratories provides the oversight and hands-on support in the form of protocols and reports.
Our clients are granted with the seamless infrastructure and dedicated team work that assures successful execution of engineering studies and design verification and validation (V&V) of medical devices and combination products.
Carmel Laboratories is ISO/IEC 17025:2005 certified by the American Association for Laboratory Accreditation (A2LA).