Confirmation letter of certification application framework of regulation (EU) 2017/745 We understand the value of transparent and clear communication with our clients, especially when it comes to compliance with regulatory standards. For all our partners who distribute our medical devic... GMED Mar 26, 2024
Vitrobio ISO 13485 certificate In our ongoing commitment to delivering safe, efficient, and reliable medical devices, we place great emphasis on adhering to globally recognized standards. A key example of this is our certification ... GMED Mar 26, 2024
Understanding the Medical Device Regulation (MDR 2017/745): A Transformative Shift in the Medical Device Industry 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 ensu... MDR Mar 26, 2024
JAN-23 : Vitrobio Certification Update 2017/745 Regulation (MDR) – Vitrobio Certification Update Vitrobio is already committed to the transition to MDR . An application for certification under Annex XI part A of Regulation 2017/745 has bee... NEWSLETTER Mar 26, 2024
OCT-23 : Vitrobio Certification Update, UDI and Changes 2017/745 Regulation (MDR) – Vitrobio Certification Update As we informed you in our July newsletter: Vitrobio is already committed to the transition to MDR. An application for certification under Anne... NEWSLETTER Mar 26, 2024
JAN-24 : Vitrobio Certification Update, Management and Ressources Dear VITROBIO Partners and Clients, The entire Vitrobio team wishes you all the best for 2024 and would like to take this opportunity to thank you for your trust and unwavering support. Our partnershi... NEWSLETTER Mar 26, 2024
EC Certificate Directive 93/42/EEC In our commitment to providing safe and efficient medical devices, we align with internationally recognized standards. One such standard is Directive 93/42/EEC (also known as MDD), a European Union di... GMED Mar 26, 2024