MedTech manufacturers can use the present guidance on medical device symbols to comply with the new, stricter MDR labelling requirements.
This post focuses on the medical device labelling requirements and user manual requirements under the EU MDR 2017/745.
This article presents three certification markings for energy-efficient products that manufacturers placing goods on the US market should consider.
This article provides clarity on what a compliance program is and what elements it consists of.
This article provides clarity on what a compliance management system is, what elements it includes and what benefits it brings to companies.