With the many processes and regulatory requirements for In Vitro Diagnostic (IVD) and Software as Medical Device (SaMD) products, it is a challenging task for any company to ensure compliance. This is a risk to both the public as well as the company, and thus it is crucial to have a system that effectively oversees these processes in maintaining the quality of products. In this workshop, hear from experts who will be discussing about manufacturing requirements, including quality management system requirements, as well as the regulatory steps necessary for a company to release the product for sale in regulated markets.  

Due to the limited availability of seats, early registration is strongly recommended.