Our Regulatory Affairs professionals are passionate about protecting the patients and consumers that they serve every day, throughout the full life cycle of our products. They ensure that our businesses design products that meet our customers’ needs, that are produced to the highest standards, and that are safe and effective. They have the confidence to make difficult decisions and know they’re working for an organization that backs up those decisions. The combination of their global policy view and their local approach to markets and customers helps them build trust and influence among customers and industry peers.

Our Regulatory Affairs professionals believe that Quality Information is more Important than Quantity of information.

The team’s regulatory experience covers the African markets, Latin American Markets , South East Asian Nations as well as a number of other global regions. Regulatory Affairs is capable of submission of Dossier / CTD / eCTD from semi-regulated to highly regulated markets.