The medical device manufacturing sector is one of the most regulated sectors in which significant quality systems and product requirements must be satisfied. The regulatory requirements are intended to ensure that manufacturers consistently design, produce, and place onto the market, medical devices that are safe and fit for their intended purpose.
We understand the specific challenges medical device manufacturers face and the importance of bringing innovative yet safe products to global markets. Ensuring the predictability and transparency of regulatory product clearance is key to maintaining a competitive edge.
BSI is a leading business services provider for organizations worldwide, offering a range of services in management system certification such as ISO 13485, product testing and certification, and standardization. Our service philosophy is focused on robust and timely reviews, making us a trusted industry regulator.