Telephone: +44 (0) 7878 722157

At Maynard Regulatory Consultancy, we help new and established companies in the medical device and IVD industry meet regulations in the UK  EU and overseas markets. We offer tailored service on matters such as regulatory strategy, compliance, quality management systems and technical documentation. No matter where you are in the development stages of your medical device, our team can offer practical advice to support your product's development journey. 

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Our goal is to help companies bring medical devices to market and maintain quality management systems whilst navigating global regulatory environments for the benefit of patients and the medical professionals that provide their medical care.