The life sciences industry is a highly regulated environment. To ensure patient safety and product reliability, Pharmaceutical and Biotech companies need to remain compliant with these regulations.

CMAST provides regulatory compliance and quality services throughout the entire life cycle of your product, from preclinical and clinical development to regulatory operations and market authorization. Post launch, we support life cycle management, quality and delisting projects.

We believe that each project is unique and we will always adapt our services to our clients’ specific wishes and needs!