Medical Devices – USA, Europe and Asia Regulatory Updates Roundup – Oct 2024
USA
Guidance on Considerations for Long-Term Clinical Neurodevelop...
Steps to Implement ISO 13485 for New Medical Device Vendors
For medical device vendors entering the industry, obtaining ISO 13...
Clinical Evaluation without Clinical Data in the EU
Application of EU MDR Article 61(10) When Clinical Data is Conside...
Medical Devices – USA, Europe and Asia Regulatory Updates Roundup – Sept 2024
USA Air Powered Dental Handpieces and Air Motors – Performance Cri...
Software IN versus AS a Medical Device
The healthcare industry has always relied on new technology to dri...
Medical Device Label Designing Important Considerations
Medical Device Labeling – an essential aspect of the Medical...
