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Harnessing continuous improvement in the CAPA process

European Pharmaceutical Review

The optimised framework aims to overall, drive higher product quality and improved patient safety. Summarising recommendations and best practices for CAPA process improvement, this whitepaper uses data collected from a pilot suggested in the MDIC’s initial whitepaper that proposed the framework.

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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.

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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.