The Product Lifecycle for Orthopedic Devices

Precision Tested:

The Product Lifecycle for Orthopedic Devices

The Medical Device Regulation (MDR) mandates that manufacturers adhere to the latest revision of relevant standards when introducing new medical devices to the market. Our team of global experts can help you comprehend the testing requirements for products at all stages of the product life cycle, including novel devices or products undergoing material or design modifications. Our newly established laboratory facility in New Brighton, MN is ISO 17025 accredited and adheres to Good Laboratory Practices (GLP), offering MRI Safety, Biological Safety, chemistry, packaging testing, reusable device testing, and routine microbiology testing for medical devices. TÜV SÜD can provide testing assistance throughout the following developmental phases.

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