Essential Terms for UK Quality Regulations Post-Brexit

August 11, 2022

Many biotechs are struggling with the uncertain state of quality regulations in the Post-Brexit UK. Understanding the new regulatory processes and requirements begins with understanding the key terms in a new MasterControl article, Joanna Blair breaks down the top 11 terms you need to know to navigate the current regulatory landscape to ensure compliance. To start, companies must know the importance of UKCA and CE markings.

According to Blair, “ The approval marking on a product shows it meets safety and quality standards, as well as legal requirements, to be marketed to consumers. For such a small marking, it represents a broad spectrum of life sciences and quality expertise that goes into the development and pre-market auditing of any health care product. Post-Brexit, manufacturers will need to add a distinct mark to any product marketed in the U.K. The European Union will continue to require its own separate marking.”

To read more, click here.

(Source: MasterControl, July 28th, 2022)

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