EU is moving from MDD to MDR. Are you ready?

5 Things You Should Do to Prepare for the New European Union Medical Device Regulation (EU MDR)

Medical devices cannot be placed on the market without conforming to safety requirements. In the U.S., the responsible regulatory agency for medical devices is the FDA’s Center for Devices and Radiological Health (CDRH). If it is a drug and device combination product, it is the CDER, Center for Drug Evaluation and Research, as well. The…

future of satellite product design

Key Considerations for Commercial Satellite Product Design

The goal of the commercial space industry is to provide fast and affordable access to space. This industry, highly regulated due to the complex nature of its products, presents unique challenges for engineers and companies. New opportunities in the industry open doors for options in product design and the influence of nimble design firms that…