Preparing for UK Medical Device Regulations: 4 Ways to Get Ready

With new guidance from the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) for regulated medical devices, companies are facing uncertainty about what to expect in the coming years. In a new MasterControl article, author Sarah Beale breaks down four strategies to jumpstart preparing for the new regulations. First, Beale recommends updating document control to help avoid headaches when EU-based certificates are no longer valid.

According to Beale, “The more changes and organizations involved, the more likely there is to be a problem with communication. Even if third parties aren’t factored in, poor document control is a regulatory hurdle. Document control software eliminates many of the problems that come from collaborating and approving documents. By having everything in a cloud-based, centralized location you can ensure that regardless of location, everyone has access to the same, up-to-date documents.”

Click here to read more.

(Source: MasterControl, February 3^rd, 2022)