DPR helped Abbott Vascular increase its ability to manufacture a new stent at their Santa Clara facility with the completion of a renovation project that included new cGMP manufacturing space in a large, ballroom-type configuration with several multi-use, multi-functional utility locations. The remodel also included support labs and offices, seismic upgrades and a new central plant.
As a validated facility, this project required a significant amount of documentation. Highly experienced in building validated facilities, the DPR team began preparing for the validation process before a single tool was picked up. By developing the documentation plan early, DPR eased the process of compiling and delivering the 40+ binder turnover package.