One of the essential commitments of VeVi Dental as a management software has been (and will continue to be) compliance with any current legislation for dental laboratories or milling centers. Thus, the market-leading software allows you to forget about the Declaration of Conformity, identification labels, or documents detailing manufacturing components. You focus on the work, and VeVi takes care of everything else to walk alongside you.

As regulations are constantly changing, your management software also evolves. In this regard, the New Regulation (EU) 2017/745 has been in force since the end of last May, referring to the surveillance of marketed medical devices. Yes, you guessed right: VeVi has met its requirements right from the very beginning.

To make everything crystal clear, here are a few key points. On one hand, the regulation requires post-market surveillance for each manufactured product. In VeVi, you will be able to include this information or other incidents in the most convenient way imaginable, so that the entire process is covered under a legal umbrella.

On the other hand, a periodic safety update report (you probably already know about the PSUR) is also required for all marketed products in order to present the conclusions of the work, possible modifications, or even issues with the final result. As usual, and with just a couple of steps, VeVi Dental will automate these tasks.

Another detail: before this regulation came into force, the software already included the locations where the prostheses were manufactured as a prominent part of the outsourcing process. This is just another example of how you stay ahead with VeVi, as we continue to work for you every single day :)