News / Blogs
Important Regulatory Update: Class I Medical Devices and CH-REP Requirements Deadline
Selling Your Medical Device in Switzerland: Best Practices and Regulatory Compliance
Is the UK MDR the same as the EU MDR?
EU MDR Device Classifications: What You Need to Know to Ensure Compliance
Navigating the New EU Regulation 2023/607 for Medical Device Compliance
Stay compliant with EU Reg. 2023/607. Expert guidance from Shiro Business Solutions - UK's top medical device regulatory consultancy
MHRA grants 1 year extension for UKCA Compliance
The MHRA announced a one year delay for UKCA Marking and confirmed a 3 to 5 year transition period for CE Marked devices this week.
