para a versão em português.
TÜV SÜD, German multinational specialising in technical certification tests, will participate in the EIT Health Regulatory Pathways to Market, a programme led by Instituto Pedro Nunes, through the Laboratory for Automatics and Systems (LAS).
TÜV SÜD, known for its experience in evaluations and compliance, will be one of the guest companies sharing its know-how during the EIT Health Regulatory Pathways to Market. The session will cover crucial topics such as the role of Notified Bodies in the European Union Medical Device Regulation (MDR) and the In Vitro Diagnostic Medical Device Regulation (IVDR). In addition, members of the German company will explain to participants the key characteristics to look for when choosing their Notified Body.
The EIT Health Regulatory Pathways to Market Bootcamp is a 10-week programme that aims to support health innovation companies and help them understand the European health services regulatory market.
The aim of this programme, which is highly specialised and tailored to the needs of these companies, is to give tools to early-stage start-ups, with a focus on medical devices and digital health, so that they can more easily access this market.
LAS has extensive experience in health technologies, medical devices, in vitro diagnostics and regulatory support. Find out more at https://www.ipn.pt/laboratorio/LAS/servico?id=2