Regulatory Affairs

Pharmaceutical product development to commercialization involves many steps which are governed and regulated by national and global Health Authorities (e.g. Infarmed, EMA, FDA, etc.). Ensuring compliance throughout the entire process is a mandatory requirement and to overlook the procedures across the product life cycle, organizations deploy proven experts for Regulatory Affairs.

The regulatory team acts as a crucial link between organization and national and global Health Authorities, tracking all the key regulations related to the product and pre-requisites for its launch.