Biomanufacturing Shows Signs of Maturity, PAT Adoption

This year, worries over cost of implementation appear to have leveled off or declined. This could mean that budget concerns are being resolved. Alternatively, PAT users and others may be recognizing the benefits that PAT can provide. The proportion identifying regulatory issues as hindrances—such as uncertainty over how regulators will deal with information generated by PAT, or that implementing PAT will increase the risk of regulatory evaluations due to small infractions or excursions—appears to be relatively steady.

Regulatory Requirements More of a Vendor Problem
Regulatory issues remain a concern for PAT adoption, and they’re also a key problem when looking at quality control in supply chain management. With PAT adoption increasing, and the frequency of batch failures decreasing, we examined what quality problems can be traced to vendors. In keeping with the positive findings from above, we find that overall, vendor problems are declining.

In fact, the only area in which significantly more respondents this year saw a problem was in vendors’ inexperience with industry’s regulatory requirements. This year, this problem was noted by 31.3% of our respondents, up from 28.1% last year, and halting a 4-year downward trend. This may reflect an increased view of the importance of regulatory factors and the perception and need to understand requirements. (The percentage of respondents complaining that vendors have not filed Device Master File on their product also increased, but only marginally, from 13.2% to 13.8%.)

Vendors are taking note of this issue, too. When we asked 185 suppliers to tell us the areas in which they perceive their clients are demanding additional support, 30.5% indicated better regulatory compliance, ranking this area higher than others such as lower prices (29.3%), better quality product offerings and better IP protection.
 
Aside from vendor issues with regulatory requirements, though, most of the other quality issues traced to vendors by biomanufacturers have declined in importance. This year, as they did last year, respondents indicated that the key problem from vendors involves making promises they cannot keep (41.3%). (See Figure 2.) Even so, the proportion citing this has fallen relatively significantly from last year, when it stood at 49.3%. Other problems that have seen significant drops include poor quality of products (just 27.5% this year, as compared to 45.6% last year and a 5-year high of 53.8% in 2010), and poor quality of service (26.3% this year compared to 34.2% last year and a 5-year high of 45.8% in 2009).

Global Quality Supply Management
The declining significance of problems traced to vendors might be a reflection of increased auditing that manufacturers are undertaking in the supply chain. We separately asked respondents to identify what, in the past 12 months, their organization has done to assure consistent quality in raw materials and ingredient supply. We found that a majority (51.4%) audited their suppliers more frequently, a relatively significant jump from 45.2% last year who were more frequently auditing suppliers. The proportion of respondents implementing more dual-sourcing also increased, from 39.4% last year to 45.9% this year.

Some factors dropped on a year-over-year basis. For example, the proportion of respondents who said that they audited secondary suppliers (those supplying their suppliers) fell from 49% to 40.5%, while this year only 36.5% implemented more comprehensive audits, down from 45.2% last year.

Even so, on a number of counts, we found that biomanufacturers are adopting more comprehensive quality supply management: More have developed new, more rigorous tests for incoming raw materials and supplies, while almost one-quarter have increased the volume of testing of incoming raw materials and supplies.

Comparing responses from biotherapeutic developers and CMOs yields some interesting divergences. CMOs, at a rate dramatically higher than biomanufacturers, are auditing their suppliers more frequently and implementing more dual-sourcing. They are also more likely to be verifying vendors’ certificates of analysis, and specifically identifying secondary suppliers.

By contrast, biomanufacturers appear to be much more active than CMOs in demanding that their suppliers demonstrate higher levels of GMP/GLP compliance, implementing more comprehensive audits, verifying the origin of individual ingredients more carefully and holding more frequent meetings with vendors.

We find a divergence in actions on a geographic basis, too. U.S. respondents are for the most part more active than their Western European counterparts in quality supply management. Some of the larger disparities we found were in: Implementing more dual-sourcing (61.1% of U.S. biomanufacturers vs. 36% of Western European respondents); and Auditing more suppliers, including secondary suppliers (52.8% U.S. vs. 28% W. Europe);

The only two areas in which Western European respondents appeared significantly more active than U.S. respondents were in auditing suppliers more frequently and testing individual ingredients.

Optimistic Picture
All told, our data paints a fairly optimistic picture. The frequency of batch failures is down to the lowest point in five years, and biomanufacturers are stepping up their supply chain quality control while complaining less of problems that can be traced to those vendors.

Despite its promise, it has been close to a decade since the FDA’s landmark guidance on PAT, and implementation remains slow and uneven, leading some to ask when this initiative will achieve its promise. Our data signals that perhaps the industry is finally ready to move to mainstream adoption of PAT. While intentions to implement may have outstripped reality in previous year, with improving economic situations and increased budgets, this may change.  The success of PAT and QbD applications in pharmaceuticals will depend on better analytics, allowing biomanufacturers to make a strong business case for using these tools to maximize yields and minimize quality defects.

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References:
1. 9th Annual Report and Survey of Biopharmaceutical Manufacturing Capacity and Production: A Survey of Biotherapeutic Developers and Contract Manufacturing Organizations, BioPlan Associates. www.bioplanassociates.com

About the Author 
Eric S. Langer is president and managing partner at BioPlan Associates, Inc., a biotechnology and life sciences marketing research and publishing firm established in Rockville, MD in 1989. He is editor of numerous studies, including “Biopharmaceutical Technology in China,” “Advances in Large-scale Biopharmaceutical Manufacturing”, and many other industry reports. He can be reached at elanger@bioplanassociates.com.

Survey Methodology
The 2012 Ninth Annual Report and Survey of Biopharmaceutical Manufacturing Capacity and Production in the series of annual evaluations by BioPlan Associates, Inc. yields a composite view and trend analysis from 302 responsible individuals at biopharmaceutical manufacturers and contract manufacturing organizations (CMOs) in 29 countries. The methodology also included 185 direct suppliers of materials, services and equipment to this industry. This year's survey covers such issues as: new product needs, facility budget changes, current capacity, future capacity constraints, expansions, use of disposables, trends and budgets in disposables, trends in downstream purification, quality management and control, hiring issues, and employment. The quantitative trend analysis provides details and comparisons of production by biotherapeutic developers and CMOs. It also evaluates trends over time, and assesses differences in the world's major markets in the U.S. and Europe.