LFH Regulatory Limited is based in Huddersfield, West Yorkshire. We offer expert regulatory, clinical and quality consultancy solutions within the Medical Device and In Vitro Diagnostic industry, from design feasibility through to product launch and post market activities. We work with you to build a regulatory framework to meet all compliance requirements, so you get your products to market quickly and effectively. We offer regulatory, quality and clinical solutions for all medical devices, including In Vitro Diagnostics. Our team have vast experience working with businesses of all sizes – from small start-ups to global manufacturers. We guide and support companies through the ever-changing regulations to ensure that each product meets the regulations and achieves accreditation. We also provide continued support throughout the lifecycle of your device, so your product not only gets to market, but stays there. In addition to global regulatory support, we also support clients with creation, remediation and updating clinical/performance evaluations. We can act as your UK Responsible Person,. We also implement and maintain Quality Management Systems and deliver in-house training. Visit our website for more details on the services we can offer.