1. Development feasibility checking for new projects.

2. Preparation project briefs for new projects.

3. Literature review and RLD identification for new products depending on
regulatory requirements.
4. Managing project pre approval activities and related documentation filings.
5. Requesting project codes for new products.
6. Providing justifications, literature and documentation support for applying
test license and import permits.
7. Calculation of shadow COGs
8. Based on projected annual volumes, calculation of tentative
developmental quantitys and forecast of API annual requirements.
9. Coordination with procurement team in identification of API source.
10.Coordination with Clinical team in identification of Bio study requirements.