Thermo Fisher Scientific Expands Steriles Manufacturing and Research Capabilities in Asia-Pacific Region
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Transforming CDMO partnerships through
Quality is the underpinning of success in the pharmaceutical development and manufacturing industry.
A commitment to quality is not only required to meet regulatory guidelines, it’s also foundational to:
- Accelerating time to market
- Reducing unnecessary risk
- Improving return on investment
- Creating effective medicines
- Ultimately saving patient lives
Despite its critical importance, quality is often mischaracterized, whether by conflating it with compliance, describing it as an end-of-the-line activity, or attributing responsibility to a single team.
In fact, quality is difficult to fully classify because it’s not defined by one single activity, role, process, strategy, or outcome. Rather, it’s a combination and culmination of all these factors — plus more.
This whitepaper takes an in-depth look at key indicators of CDMO quality, identifying tools and best practices to drive continuous improvement, strengthen collaboration, and ultimately cultivate trust.
