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.

How the Executive Certificate Workshop: Manufacturing and Quality Management System can benefit your career

In this workshop, you will hear from experts discussing key manufacturing requirements, including quality management system standards, and the regulatory steps needed for a company to release a product for sale in regulated markets. This workshop will provide valuable insights into navigating the regulatory landscape for product launch.

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

Click here for a step by step guide on how to register.