Enhancing Compliance through Novel Approaches to Commissioning & Qualification

Rubrik: Biotechnologie

(Treffer aus pharmind, Nr. 09, Seite 1304 (2017))

Urban B | Musa T | Smith R | Grønnegaard J

Enhancing Compliance through Novel Approaches to Commissioning & Qualification / Validation (CQV) of Automation, Facilities, Utilities, and Equipment Systems used in Biologics Manufacturing · Urban B, Musa T, Smith R, Grønnegaard J · ¹Biogen, Research Triangle Park, USA und ²Biogen, Hillerød, Denmark
Historical approaches to automation, facilities, utilities, and equipment qualification mitigated risk through large amounts of documentation and testing. The foundation of the next generation approach is driven by a risk profile (e.g., ICH Q9 (Quality Risk Management)), which clearly defines how to verify that the aspects of systems that impact patient safety, product quality, or drug supply are qualified for use. Thus, challenging the status quo of the traditional automation, facility, utility, and equipment qualification strategies – while maximizing the assurance of quality and compliance.