Biovica completed meeting with the FDA

2019-07-25 12:16

On the 22nd of July, Biovica had fruitful meeting with the FDA regarding Supplement II that discusses the approach for clinical validation of DiviTum.

Next step is to document the conclusions from the meeting, which the FDA will review and signoff. This process will take a maximum of 45 days.

Thereafter, Supplement II will be completed, and the result can be concluded and communicated.

Some of our Collaborations

>3200

Numbers of patients in studies

24

Publications

10

Pharma Contracts