Maintains personnel files, conduct audits to ensure the files are accurate and complete.

Identify new assets/companies/areas of innovation through industry and academic network.

• Manage on-going clinical study. • Provide clinical/scientific inputs during the development and execution of clinical trials

The Director, Regulatory Affairs provides Regulatory support to the development team to ensure that the development plan provides for the highest Regulatory probability of success.

Provide strategy for rapid and timely approval of new products and regulatory support for clinical products globally–early identification of regulatory challenges throughout clinical development.