Regulatory compliance is a necessity in the development of medical devices such as In Vitro Diagnostic (IVD) and Software as Medical Device (SaMD) to safeguard the health and safety of patients when used as intended. This is pivotal to an effective product life cycle management. 

This workshop will build upon concepts on Design and Development and look into how manufacturing requirements are determined. These procedures are essential to ensure that products developed during the design phase can be manufactured, and contribute to the successful planning of product registration activities.

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