Whether you are a few products manufacturer or with 1000s of SKUs, regulatory data and tracking are challenging. Whether through your homegrown tools or Excels or QMS or PLM/ERP, effective planning, tracking and managing of registrations info is not easy. With more Health Authorities moving to Digital from the Document world, it’s not an option of “if” but rather “when”.
Med Device companies’ challenges are different and unique compared to BioParma companies. ViSUis focused on MedTech companies.
Registration management solution for medical devices allows product registration tracking to significantly reduce the risk, effort, and cost of managing global submissions. It assists med device manufacturers to manage new and product life cycle activities effectively.