Pfenex Responsibilities. Promptly after the filing of the Regulatory Documentation with the FDA, but in any case within thirty (30) days of such filing, Pfenex shall deliver to Alvogen a copy of such Regulatory Documentation, provided that Alvogen and any Sublicensee may only use such Regulatory Documentation and the Know-How incorporated therein pursuant to the Product License, including the right to use such Regulatory Documentation for compiling Regulatory Materials.
Appears in 2 contracts
Sources: Development and License Agreement (Pfenex Inc.), Mena Development and License Agreement (Pfenex Inc.)