We supply help and advice on regulatory affairs and quality assurance. We specialise in medical equipment or medical devices, and in particular the EU requirements. We work in all aspects of the regulatory submission process at levels of intervention which the client decides. From strategic advice and remote support right through to interim management. We work with start-up companies to globals.

Impregnated throughout our work, like a watermark on paper, is the phrase ‘business solutions.’ We are equally committed to our ethical statement.

We also offer comprehensive EU Authorized Representative Services. The same pedigree of ‘business solutions' extends to this service, and being based in the UK is ideally placed to provide services to English-speakers worldwide.

Being EU based, the main focus of Priory Analysts is on medical device CE marking. However, we regularly undertake commissions for approvals in other regulatory jurisdictions. We either do these ourselves, or through a network of tried and trusted associates who share our core values.

See our product list.