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.

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What we do:

Don’t decide between product quality and production efficiency.

You can have a more efficient, more sustainable, lower cost facility that produces the best quality pharmaceutical products for your patients. Get a customized, best-in-class solution from experts who possess extensive knowledge and experience in all aspects of pharma manufacturing.

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Make APIs faster, cheaper and with less waste.

It’s not enough to build a functional bulk pharmaceuticals manufacturing facility; you must meet increasingly more rigorous safety and quality standards, while producing APIs quickly and efficiently. Get a solution for your new or existing facility to achieve your business aims, and most importantly, find opportunities to improve upon your process.

Reduce your animal health project timeline and lower capital costs with lead design and construction execution.

Animal health affects billions of people worldwide, so it’s vitally important that your products are effective and safe. How do you do that when the cost margin is low?
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Improve your plasma fractionation processing with innovative solutions.

Clean, streamline and simplify your bulk processing facility with the right design and regulatory expertise. From process utilities to equipment, get a solution that includes the mixing, liquid transferring and chilling, filtering and clean-in-place considerations needed to maximize your cleanability and efficiency, while minimizing operator intervention. No matter the extent of your project, our team builds value into your human plasma-derived therapeutics facility by finding the best opportunities to improve your outcomes while ensuring compliance to applicable codes.

Revolutionize oligonucleotide manufacturing for life-changing therapies.

As more drugs achieve FDA approval and demand increases, position yourself for rapid expansion. Successfully make the transition to commercial scale.

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Patients are relying on your OSD drug product.

Because a well-designed process is central to your success, the right process solution is also unique to you. Whether you’re ready to enter the continuous manufacturing arena or you’re looking to achieve a wider range of capabilities with a more robust CM system, implement the process that’s best for your business.

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