Through working in the industry for many years, we have developed extensive knowledge and expertise in all areas of medical device development. Working with businesses and manufacturers of all sizes, we specialise in:
Make sure that your medical devices are fully compliant and offer the most effective assistance possible for users with the help of our consultants. Patient Guard Ltd is a medical device consulting business in Blackpool, Lancashire, that primarily focuses on regulatory affairs and quality assurance. It is our aim to help you with the regulatory and quality compliance of your medical devices, no matter if you are an inventor, start-up company, SME, or larger business. To support you in all aspects of medical device development, we have a wide network of contacts and more than 13 years of experience, including time spent working with notified bodies and the MHRA.
Set up in 2017, and based in the North West of England, we are striving to quickly become a regional and national centre of excellence and your partner of choice when it comes to your medical device development and post-marketing needs. To achieve this, we will offer quality expertise and experience within the field in a no-nonsense, straightforward way that suits your business needs. Already we have a proven track record as well as many contacts, including:
What’s more, for your peace of mind, we are a proud member of the LRQA’s Consultants Network and The Organisation for Professionals in Regulatory Affairs (TOPRA).