Different dosage forms have different effects on clinical outcomes. Advanced dosage forms may have higher quality and technical requirements for its excipients. Unibest cooperates with China Pharmaceutical University-Aoqi Biotech Joint Research Institute, works closely with experts, and hope to overcome formulation difficulties.

Unibest is always ready to declare registration in both the Chinese and global markets for our partner to focus on the capacity of the formulation team. We have the authority and specialists for regulatory registration for formulation. So far, we have completed more than 10 product registrations and also absorbed experts from CDE, NMPA, etc., as our registration/QA advisors. With Unibest, it is not hard to bring your good products to the stage.

Unibest is always ready to declare registration in both the Chinese and global markets for our partner to focus on the capacity of the formulation team. We have the authority and specialists for regulatory registration for formulation. So far, we have completed more than 10 product registrations and also absorbed experts from CDE, NMPA, etc., as our registration/QA advisors. With Unibest, it is not hard to bring your good products to the stage.

The process of license in and out for FDF & API, including Technology development and marketing strategy design, are long and complicated. Unibest have a special project team led by experienced advisors who understand the latest policies and propose strategic cooperation plans to mitigate related risks.

Quality assurance is an entire system Unibest can supervise the entire process from R&D to sales. We are trying to guarantee the quality of the R&D process and dosage quality and decrease the negative review rate by tracking and managing from time to time.

Whether looking for multi-channel agents or technology transfer, Unibest will transform registered drugs or technologies into mighty market power through advanced channels. We believe that Unibest's products are oriented to the present and the future, and we also hope to realize our vision through our technical and product-side capabilities "enable good medicine worldwide."

The process of license in and out for FDF & API, including Technology development and marketing strategy design, are long and complicated. Unibest have a special project team led by experienced advisors who understand the latest policies and propose strategic cooperation plans to mitigate related risks.

Quality assurance is an entire system Unibest can supervise the entire process from R&D to sales. We are trying to guarantee the quality of the R&D process and dosage quality and decrease the negative review rate by tracking and managing from time to time.

Whether looking for multi-channel agents or technology transfer, Unibest will transform registered drugs or technologies into mighty market power through advanced channels. We believe that Unibest's products are oriented to the present and the future, and we also hope to realize our vision through our technical and product-side capabilities "enable good medicine worldwide."