Patient Guard is a Medical Device consultancy business focusing on EU Regulatory Affairs and Quality Assurance. Based in the North West of England we strive, to be your partner of choice when it comes to your Medical Device Regulatory and Quality Assurance requirements. We appreciate the regulatory landscape can be a difficult one to navigate, and for companies trying to get a product to market can be frustrating, knowing what is required, what it entails and how much it will cost can be difficult information to find out. Patient Guard will guide you though the process and be upfront with the commitment that will be required, we will provide a detailed analysis and estimated costs for what ever stage of development you are at. Patient Guard can support you though out the life cycle of your medical device being placed on the market, including your post market and vigilance requirements. Visit our website to find out more and make an inquiry, we will offer a free consultation to find out your needs and see where we can help you.