Medical device testing the bdc labs team has over 35 years of experience in medical device product research development and testing.
Medical device testing services.
At tüv süd we combine expert medical product testing knowledge with a global network of internationally accredited laboratories and facilities providing you with a one stop solution.
State of the art medical device testing.
Medical device testing services qualified staff specializes in providing well defined protocols and fixture design.
Operational compliance and accreditation glp olaw aaalac.
Our focus is on functional engineering based testing of medical devices including class 2 and class 3 devices.
One stop expertise in medical device testing.
Partner with us and gain a reliable medical device testing lab expert seamlessly at your side.
Eurofins medical device testing provides global medical device testing services for medical device companies of all sizes.
We are over 700 scientists technicians and service specialists diligently performing more than 400 rigorous tests in 11 global laboratory locations.
Imr test labs is an accredited materials testing lab providing analytical services to the medical device and dental industries.
Medical device and materials testing including safety assessment through extractables leachables and bioanalysis supporting all stages of development and manufacturing.
Mdt services also offers test performance and accurate reporting to the medical device testing community.
Commonly referred to as biological safety this evaluation of risk consists of the biocompatibility component but also multiple other.
Medical device testing is a critical step in the process of transforming an innovative design into a reliable and marketable product.
Clinical research services multi disciplined clinical teams who provide robust gcp and iso 14155 compliant clinical trials for low risk medical devices.
Open paradigm of collaboration as a non profit 501 c 3 institute.
Biocompatibility of medical devices.
We profile the safety and efficacy of implanted devices and combination products and develop novel testing and assessment procedures with multiple regulatory compliances.
The biocompatibility of medical devices directed by iso 10993 1 is a critical part of the medical device risk management process.
We have extensive experience working with medical oems to verify raw materials handle overflow testing from internal labs test finished products and provide support to research and development efforts.