par Administrateur | Août 3, 2023 | Regulatory
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 directive that sets the framework for marketing medical devices. To...
par Administrateur | Août 2, 2023 | Newsletters
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 been submitted to the GMED, for the entire product portfolio....
par Administrateur | Août 2, 2023 | Non classé
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 to ISO 13485, an international standard that specifies requirements...
par Administrateur | Août 2, 2023 | Regulatory
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 devices, we want to provide assurance of our commitment to meeting the...
par Administrateur | Juin 20, 2023 | Regulatory
Understanding Medical Devices, their Classes, Market Dynamics, and a Deep Dive into the Production of Class IIa Nasal and Throat Sprays Medical devices form an integral part of the healthcare industry, spanning from simple tools like bandages to complex...
