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    Quality risk management (QRM) is a systematic process that assesses risk to the quality of a drug product. Our coverage in this area is specific to thetools and techniques, such as CAPA and HACCP, used to help pursue a quality strategy.

    Articles

    Michael Annino | Shutterstock-AI
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    How pharma can use CAPA as a tool to support continuous process improvement
    How intelligence-driven solutions can refine pharma’s quality operations
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    Adopting a risk-based model for inspections will flag suppliers who aren’t up to par
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    CAPA remains an integral element of cost-effective quality management in pharma
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    CPV is required for regulatory compliance but can also provide process improvements
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    With the use of self-service analytics, process engineers have full control over COVID-19 vaccine production and quality
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    More companies are implementing MES to improve quality at every step – and get products to patients faster
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    What every quality leader should look for in a digital platform for pharma manufacturing
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    New AI applications make it possible to automate much of the corrective action/preventive action process
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    How new techniques and more versatile equipment can improve syringe inspection
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    Inside Piramal Critical Care’s search for equipment that could meet the unique needs of its anesthetics products
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    How advances in biopharmaceutical characterization technologies are improving drug quality
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    Digital and automation technologies have created opportunities for change in pharma QC laboratories
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    Atrium improves audits and complaints, change control, and product release processes with immediate access to information and operational visibility