Analyzing the Best Fit for a Facility - A brief case study of a facility-fit analysis provides insight into how to adjust capacity when moving from clinical-to commercial-scale production. - BioPharm

ADVERTISEMENT

Analyzing the Best Fit for a Facility
A brief case study of a facility-fit analysis provides insight into how to adjust capacity when moving from clinical-to commercial-scale production.


BioPharm International Supplements
Volume 25, Issue 11, pp. s33-s36

Understanding the facility's original capabilities

Although reasonably flexible, B633 had been originally designed to manufacture only one to two commercial products per year. With MedImmune's changing business focus and robust pipeline, the company now had to target multiple late-stage clinical candidates and fixed commercial requirements on an annual basis. By analyzing the long-term clinical and commercial demands on the facility, not just manufacturing capacity but also technical transfer and postmanufacturing support, a team was able to identify immediate areas of opportunity to increase capacity. Additionally, longer-range initiatives were identified.

First, the company modeled the plant and processes to identify potential bottlenecks. Because the manufacturing plant was now required to run multiple products, archetypical processes were developed that reflected the range of titers that could potentially occur with the product portfolio. Large-scale manufacturing plants such as B633 are designed with a certain amount of throughput. The throughput of the plant is a function of run rate. The capacity of the plant is driven by a combination of run rate and plant idle time. The idle time of the plant basically resides in two areas, one being the time to evaluate and characterize products that have been first introduced to the plant and scaled to 15k bioreactor scale and the other being plant changeover from one product to the next. In case of product evaluation, most commercial manufacturing facilities do not require the time to evaluate products between batches; therefore, this switch is not a significant factor influencing capacity. However, this element represents greater influence in a late-phase clinical program where scaling the process beyond the pilot plant level is common practice.

Likewise, product changeover can be fairly influential in determining overall plant capacity. For example, if a changeover process requires 10 days, then one has to consider the impact on available overall plant capacity if it has two products going through the facility per year versus five products. In the former case, one could attribute plant changeover to a 20-day reduction in plant capacity. In the latter case, 50 days of capacity are lost to changeover time. Some key questions emerge: What does capacity look like in the current state versus the optimized state? And how aggressively can changeover time be improved to increase throughput?

MedImmune examined ways to reduce the second component of idle time—that is, product evaluation. In this case, a team developed a risk-based approach to evaluate and characterize products with the goal of minimizing the time between batches. The ability to model and demonstrate consistency of scalability from bench to commercial scale for the bioreactors provided a high degree of assurance that product quality would not be impacted as the process is scaled.

During the processing of the initial batch from a campaign at scale, the team gathered further evidence by conducting laboratory scale purification studies to evaluate harvested material from the production reactor for product compared with material produced earlier in the development cycle at the pilot scale. This analysis typically occurs simultaneously with the large-scale purification process and data from the "scouting study" is available prior to the end of the large-scale purification.

Lastly, the team looked at ways to minimize differences in the overall production process required for multiple products. Rather than investing time and money focusing on changing the facility itself because the manufacturing processes are different, the team evaluated the option of approaching each new product candidate employing a common process that can be broadly used for a range of products in the development portfolio. The use of this platform-process approach by process development enables the site to meet the goal of minimizing changes to the facility to accommodate new products.


blog comments powered by Disqus

ADVERTISEMENT

ADVERTISEMENT

AbbVie/Shire Deal Officially Off
October 20, 2014
Amgen Sues Sanofi and Regeneron over Patent for mAb Targeting PCSK9
October 20, 2014
EMA Works to Speed Up Ebola Treatment
October 20, 2014
Lilly to Close Manufacturing Facility in Puerto Rico
October 17, 2014
BioReliance Introduces New Predictive Assays
October 17, 2014
Author Guidelines
Source: BioPharm International Supplements,
Click here