LFH Regulatory is your trusted partner in navigating the complex world of medical device and In Vitro Diagnostic Regulations. We work clients to build a regulatory framework to meet all compliance requirements, so they can get their products to market quickly and effectively. We offer regulatory, quality and clinical solutions for all medical devices, including In Vitro Diagnostics. Our team has 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 the creation, remediation, and updating of clinical and performance evaluations. We can act as your UK Responsible Person. We also implement and maintain Quality Management Systems and deliver in-house training.