Medical Device Testing Laboratory

We are over 700 scientists technicians and service specialists diligently performing more than 400 rigorous tests in 11 global laboratory locations.

Medical device testing laboratory.

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. Commonly referred to as biological safety this evaluation of risk consists of the biocompatibility component but also multiple other mechanisms that work together to accurately predict medical device biocompatibility based on individual materials and use. Medical device testing is a critical step in the process of transforming an innovative design into a reliable and marketable product. With 20 laboratories in north america europe and asia pacific eurofins medical device testing offers regulatory compliance expertise and experienced gmp glp iso 17025 testing to ensure rapid turnaround times with the highest level of service and most advanced technologies for your analytical chemical microbiological biocompatibility electrical mechanical.

Mdt services also offers test performance and accurate reporting to the medical device testing community. Your global testing partner. Medical device testing services qualified staff specializes in providing well defined protocols and fixture design. Our medical device experts share their testing tips and best practices.

Often overlooked is the tremendous amount of research typically years that goes into developing medical devices. One stop expertise in medical device testing. Centrifuge for testing blood in a laboratory. This dramatically altered the medical device industry and ultimately gave rise to nelson laboratories.

Ddl has nearly 30 years of first hand experience navigating complex testing standards and medical device industry regulations and holds a reputation for extraordinary responsive service. The biocompatibility of medical devices directed by iso 10993 1 is a critical part of the medical device risk management process. The pharmaceutical and medical devices agency pmda is an independent administrative institution responsible for ensuring the safety efficacy and quality of pharmaceuticals and medical devices in japan. Preparing for a medical device testing program can be a challenge for many manufacturers especially if it is a new or novel product or if time is limited.

One of the major functions of this agency is to review marketing applications of medical devices and in vitro diagnostic ivd products. Biocompatibility testing of medical devices standards specific information for the accreditation scheme for conformity assessment asca pilot program guidance for industry. Laboratories may be public or private dedicated research sites located at oem facilities or on college.