Genevoyager has a team of experienced drug registration and project management with rich professional knowledge and good communication and collaboration ability, familiar with various regulations and policies, review requirements and filing process, can provide you with drug development and registration strategy consulting, new drug IND, BLA and other CTD format material writing and filing services to assist customers to successfully achieve drug registration.

Deliverables: Process development reports, COA, batch production records, batch inspection records, as well as analytical method validation, stability studies and other related CMC materials, complete the writing of CTD format declaration materials, declare IND/NDA/BLA.

If you would like to know more, please contact us.