Free Sales Certificate (FSC) for Medical Devices in India
INTRODUCTION If you’re a medical device manufacturer in India looking to export your products, one crucial document you’ll need is the Free Sales Certificate (FSC). But what exactly is an FSC, and how can you obtain it for your products? This guide will walk you through the process, requirements, and everything you need to know […]
MHRA Device Registration Guidance Update 2026
The MHRA (Medicines and Healthcare products Regulatory Agency) has recently released updates and announcements regarding medical device registrations and regulations for Great Britain (GB) and Northern Ireland (NI). These changes are expected to impact manufacturers, UK Responsible Persons (UKRPs), and the UK Medical Device Registration processes, with specific implications for both new and existing devices. […]