par Administrateur | Juin 20, 2023 | Regulatory
Implications of the Extended Transition Period and How it Impacts Legacy Devices and Their Marketing Authorization The evolution of the regulatory landscape in the medical devices sector has witnessed a notable transition from the Medical Devices Directive...
par Administrateur | Juin 19, 2023 | Regulatory
Exploring the Origins, Implications, and Future Impact of the MDR for Stakeholders in the Healthcare Sector The healthcare landscape is ever-evolving, with regulatory frameworks often adapting to ensure safety and efficacy of medical devices. One such...
