Mitigate the risks of your most complex aseptic processes.
Sterile drug products leave little margin for error.
With stakes this high, you need complete assurance that your aseptic process is safe.
Every component matters in aseptic processing—especially the people designing and building your facility. The safety and efficacy of your product relies on the coordination and interaction of personnel, equipment, facility and the product. Cleanliness and contamination control must be engineered and built in.
How can CRB help you?
Get the critical knowledge needed for these critical processes. From aseptic technique to cleanroom design and construction, we have the foremost experts in aseptic and sterile product manufacturing. We are actively involved in the regulatory bodies, and participating not only in the implementation of Annex 1, but also educating others on the update.
Your aseptic technique, fill finish procedure, equipment, controls and facility will come together seamlessly to produce pharmaceutical drug products that you—and patients—can trust.
For safe, efficient aseptic processing, call on CRB.
Let’s tackle your next project.
Download Now – Horizons: Life Sciences
Our 2022 edition of the life sciences report, built on the insights of nearly 500 industry leaders, explores the transformative change this field is poised to undergo in the wake of the pandemic and ever-increasing investment in R&D.