Managing unexpected events in the manufacturing of biologic medicines

11Citations
Citations of this article
46Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The manufacturing of biologic medicines (biologics) requires robust process and facility design, rigorous regulatory compliance, and a well-trained workforce. Because of the complex attributes of biologics and their sensitivity to production and handling conditions, manufacturing of these medicines also requires a high-reliability manufacturing organization. As required by regulators, such an organization must monitor the state-of-control for the manufacturing process. A high-reliability organization also invests in an experienced and fully engaged technical support staff and fosters a management culture that rewards in-depth analysis of unexpected results, robust risk assessments, and timely and effective implementation of mitigation measures. Such a combination of infrastructure, technology, human capital, management, and a science-based operations culture does not occur without a strong organizational and financial commitment. These attributes of a high-reliability biologics manufacturer are difficult to achieve and may be differentiating factors as the supply of biologics diversifies in future years. © 2013 Springer International Publishing Switzerland.

Cite

CITATION STYLE

APA

Grampp, G., & Ramanan, S. (2013, August). Managing unexpected events in the manufacturing of biologic medicines. BioDrugs. https://doi.org/10.1007/s40259-013-0018-5

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free