With the ever increasing regulatory challenges drug manufacturers are facing, creating documentation for your pharmaceutical products on your own can be costly and time-consuming. That’s why we developed our EMPROVE® qualification.
With a portfolio of 400 raw materials, Merck Millipore helps you obtain the documentation and approvals you need to bring your products to market faster than ever. Backed by our proven expertise and reputation for uncompromising reliability you can avoid potential error sources of manual documentation.
Speed approval preparation for faster time to market
Time and money savings
Create formulations with full regulatory compliance
Merck Millipore's EMPROVE® portfolio includes the following product lines:
EMPROVE® api: For use as an active pharmaceutical ingredient
Our EMPROVE® dossiers comprise detailed, usage-specific documentation that includes information on manufacturing, test methods, purity and stability data, helping you to successfully navigate regulatory challenges.