The Quality and Regulatory Affairs Department has the primary responsibility to ensure that all products manufactured by FIDSON HEALTHCARE PLC, are of the desired quality and that the product meets the regulatory standard (Both local and International) as well as meet and exceed the expectations of its consumers and customers. The Department ensures manufacturing processes and the way of working are in compliance with the principles and requirements of current Good Manufacturing Practices (cGMP) and best practices in the industry.

The Department provides effective and efficient quality services, to factory operations and other departments in the organization, that support internal business processes while at the same time delight the external stakeholders.