In a world of regulatory compliance, there has never been a more important time for the healthcare industry to address product information management. Patient safety, medical device traceability and government regulations are having a profound effect on product information within the healthcare industry.
The demands are growing and it is essential that healthcare companies find a comprehensive and cost-effective approach to manage, collect, validate and distribute information.
The healthcare industry is evolving and the ability to control trusted quality data can be challenging.
If you manufacture or supply medical devices or pharmaceuticals, then you’ll need to comply with multiple regulations in the near future. Whether it’s for the public sector (NHS in the UK), Group Purchasing Organizations, Regulation in Europe (MDR and IVDR) or in the US (FDA GUDID) – there are strict new regulations and customer demands you must meet in order to continue to do business. Continue reading