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    When nonconformities strike: how to stay compliant with Scilife

    Capture and close deviations and nonconformities before they turn into regulatory red flags. 

    Agenda

    04:10
    Introduction


    15:05
    Challenges

    25:35
    Case Study and Demo of nonconformities with Scilife eQMS


    54:35
    Q&A

    Join Jordi Ametller, Account Executive, and Angel Buendía, Knowledge Manager, to learn how Scilife’s Events Solution ensures full traceability and compliance with ISO 13485:2016 and GMP. Featuring a real-world case of a medical device manufacturer detecting, recording, investigating, and resolving a component failure through a connected digital workflow. 

    You’ll learn how to:

    • Manage documents with full traceability and 21 CFR Part 11–compliant e-signatures
    • Streamline approval workflows and SOP distribution
    • Apply print control where paper copies are still required
    • Assign and track trainings automatically by user functions
    • Create and assess trainings, from Read & Understood acknowledgments to quizzes and videos