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Innovation pharmaceutical tools

The unique properties of highly fluorinated materials are thus expected to continue inspire chemists, offer new research tools for the life sciences, and contribute to the emergence of new diagnostic and therapeutic innovations. Pharmaceutical development involves increasing complexity and heavy regulatory, financial, and other constraints, and time. Managing such complexity... [Pg.480]

Our failure risk analysis and opportunity method and iterative software tool, as part of our New Product Process Innovation (NPPI) Tool Library, promotes systematic collaboration and team-oriented engineering thinking when a new pharmaceutical manufacturing system process and/or product are developed. (We call it opportunity method too, since most risks, if not all, offer new opportunities for innovation.) It is based on our generic process failure risk analysis method that could be apphed to literally any process that involves risk—and innovation is a very risky process. [Pg.183]

Holdford DA, Kennedy DT. 1999. The service blueprint as a tool for designing innovative pharmaceutical services. [Pg.357]

The pharmaceutical community was asked take on the responsibility for developing standards to support the introduction of innovative tools and technologies under the PAT framework. The ASTM International provided the process to develop these standards using technical expertise in all relevant disciplines from the pharmaceutical community and other industrial sectors. A significant support infrastructure for the desired state is emerging in several academic and scientific organizations and associations. [Pg.489]

Innovation Risk Analysis and Opportunity Method and Tool with Pharmaceutical Manufacturing System Applications... [Pg.165]

INNOVATION RISK ANALYSIS AND OPPORTUNITY METHOD AND TOOL WITH PHARMACEUTICAL MANUFACTURING SYSTEM APPLICATIONS... [Pg.183]

It should be evident that concurrent validation is especially useful as a QA tool. This approach to validation is useful to QA because it enables QA to set its own objectives as criteria for PV. For example, QA seeks to have every process validated. Most pharmaceutical products contain one or two active ingredients. Process validation is very straightforward for them however, a whole new situation exists for a multivitamin/multimineral product. Innovative techniques are thus needed to achieve adequate validation. [Pg.810]

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