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Harnessing continuous improvement in the CAPA process

European Pharmaceutical Review

With the corrective and preventive action (CAPA) process often a “one-size-fits-all” approach, a whitepaper by the Medical Device Innovation Consortium (MDIC) Case for Quality Collaborative Community (CfQcc) has instead shared a risk-based framework focusing on continuous improvement. These results are included in most recent paper.

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Environmental Sustainability in Biopharmaceutical Facility Design

ISPE

linear) design process is central to successfully attaining such comprehensive sustainability goals and project needs (see Figure 1). Transforming Our World: The 2030 Agenda for Sustainable Development.” 7 An integrative (vs. 1 Circular Economy Practitioner Guide. Accessed 3 December 2022. www.ceguide.org/ 2 United Nations.

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Considerations for a Decentralized Manufacturing Paradigm

ISPE

Worldwide Modular Facilities in Pharmaceutical and Biotechnology Industry to 2030 - Impact Analysis of COVID-19.” www.prnewswire.com/news-releases/worldwide-modular-facilities-in-pharmaceutical-and-biotechnology-industry-to-2030 impact-analysis-of-covid-19-301332565.html AAPS PharmSciTech 23, no. 6 (2022):215. 39 PR Newswire.