Optimizing Immunoglobulin Production

Optimizing Immunoglobulin Production

Having previously collaborated to build a plant to produce human blood plasma-derived immunoglobulins in Bern, Switzerland, GEA and CSL Behring partnered again to commission and install further equipment in a second facility in Melbourne, Australia.

Manufacturing Immunoglobulins

GEA and CSL Behring first worked together to create the first module of a plant to produce the human blood plasma-derived immunoglobulin (IVIg) drugs Privigen® and Hizentra® to treat patients with serious and rare conditions such as immune deficiencies. Based on the success of that project, module two was commissioned and the companies teamed up again to design and build a third module in Melbourne, Australia.

The R&D department in Bern had been working hard to improve the immunoglobulin manufacturing process and, as a result, it was decided to integrate this development into the current production system. This meant scaling-up the laboratory process to production scale while maintaining the yield. Having led the previous three projects, one of GEA’s expert Project Managers was the obvious choice to steer this upgrade as he knew the systems very well and initiated the basic and detail engineering work.

“We provided all the mechanical engineering,” he explained, “including P&IDs, equipment lists, tank workshop drawings, 3D designs, time schedules, mechanical installation qualification (IQ) and the relevant technical documentation.”

He added: “As well as supplying nine pharmaceutical production tanks with all the required valves, pumps, pipelines and instrumentation, we were also contracted to provide the mechanical installation of the system, which was handled by our experienced assembly engineers. During the ‘hot’ phase, we had 20 fitters on site to ensure that we met the customer’s tight time schedule.”

The Project Manager said that the most difficult part of the project was just before an upcoming holiday period, when all the work had to be done prior to the biannual two-week maintenance break, to prepare the connections between the existing plant and the new one.

“That was a tough time,” he said: “For almost a whole month, the whole team worked without a break. But, by using small assembly groups that worked well together and remained flexible, we were ready in time.”

Before the vacation, the Project Management and his team made the connections to the existing system using the cleanrooms that were not in use during the break. “We began to identify all the necessary connections and work packages to define the requirements for the fitters and welders during the break, as well as the engineering resources that would be needed to qualify the newly installed equipment,” he explained.

This IQ check includes ensuring that all the connections comply with the approved P&IDs, the valves are in the right place, the slope of the pipes is within tolerance, all the water pressure tests are successful, there’s no leakage or pressure loss, the welding documentation is correct and complete, and the pipeline isometrics comply with the installation.

The GEA team worked closely with the customer and the automation company during this phase. After the holiday, production returned to normal without any problems or product losses. And, one month later, the project was complete and CSL Behring was able to safely commission the new plant alongside the existing system, ready for full production.

Highest Product Quality

Drug production and the manufacture of active pharmaceutical ingredients (APIs) demands the very highest product quality and purity standards, as well as validated manufacturing processes. As a supplier of sterile process plant with many years of experience, GEA can draw upon the comprehensive theoretical knowledge and expertise of its engineers to provide you with modern, bespoke and cost-effective process technology to manufacture new medicines according to cGMP guidelines and both US FDA and EMA requirements.

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Based on tried and tested standards, our project teams will devise project documentation that’s specific to your individual requirements and competently deliver the project on time, on budget and to the agreed level of quality.
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