Fully Utilizing Closed Systems in Modern BioPharma Facilities

Build the roadmap to biopharmaceutical manufacturing and their partners in developing, assessing and verifying unit operations leading to an appropriate facility design that is “right classified”. Hear first-hand about this industry-developed document to understand the tools, steps and documents required to adequately risk assess and qualify modern facilities that make use of modular, closed technology.

Learn how following a methodology results in significant gains in reducing the time to deliver the facilities and CAPEX and OPEX costs.