Clinical Manufacturing

Vanton is experienced in preparing Pre-IND package that is compliant with FDA’s guidelines and Client’s demands. Balances between these two organizations requires understanding of the project, techniques, and the FDA regulations.

Vanton posts all potential regulatory questions and runs through thorough rehearsal with clients to ensure questions raised to the agency are appropriate.

Vanton Labs can help you move your product development forward.

Copyright © 2015, Vanton Research Laboratory, LLC. All rights reserved.