City: Lancaster

With extensive knowledge of the commercialization process, regulatory requirements and scientific trends in the Industry, 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 and package testing needs. Our scientists and engineers have been assisting companies, large and small, with developmental testing for more than 40 years; and our global network of >20 laboratories in North America, Europe and Asia Pacific provide extensive capacity and the highest level of instrument technology with a full scope of testing services. | Eurofins Medical Device Services, with its network of 20+ laboratories around the globe, provides world class medical device consulting, testing, and sterile packaging (design, manufacturing, sterilization, and testing) to GMP/GLP/ISO 17025 standards. With a 40+ year reputation of client service excellence through industry-leading turnaround times, advanced technologies, and regulatory rigor, medical device developers and manufacturers trust Eurofins for at all phases. | With extensive knowledge of the commercialization process, regulatory requirements and scientific trends in the Industry, 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, mechanical and package testing needs. Our scientists and engineers have been assisting companies, large and small, with developmental testing for more than 40 years; and our global network of >20 laboratories in North America, Europe and Asia Pacific provide extensive capacity and the highest level of instrument technology with a full scope of testing services. | From implants and instruments, to single-use and combination products, as well as active electronic devices, Eurofins Medical Device Services network of laboratories provides the optimal testing strategy for all types of class I, II and III medical devices and are dedicated to helping you verify and validate your product designs; confirm safety and efficacy; and ensure user needs are met. With extensive knowledge of the commercialization process, medical device preclinical testing, international regulatory requirements, and scientific trends, our scientists and engineers have been assisting companies, large and small, with developmental testing and regulatory submissions for more than 40 years. Our >20 state-of-the-art medical device services facilities throughout North America, Europe and Asia Pacific offer extensive capacity and the highest level of instrument technology, enabling us to provide the full scope of testing services required by the Medical Device Industry, including Analytical Chemistry, Microbiology, Biocompatibility, Electrical & Mechanical, Packaging and Stability Testing & Storage. With an unwavering commitment to global regulatory standards, Eurofins Medical Device Services network of laboratories can help develop and execute all types of medical device testing plans, and navigate the regulatory pathway to market anywhere in the world. We maintain quality systems compliant with cGMP, GLP and ISO 17025, and conduct testing in accordance with ISO, ASTM, ANSI, AAMI standards, as well as custom test methodologies to meet our customers’ unique challenges. Eurofins Medical Device Services is a brand used by several distinct legal entities, across a global network of more than 20 laboratories across North America, Europe and Asia Pacific.