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    How CDMOs can win sponsor trust with an audit-ready QMS

    Learn how to stay consistently audit-ready and meet sponsor expectations with Scilife.

    Agenda


    04:40
    Introduction

    12:21
    Benefits of Scilife's eQMS for CDMO business

    16:58
    Challenges CDMOs

    28:30
    Demo with Scilife eQMS

    59:00
    Q&A Session

    When pharmaceutical companies consider Contract Development and Manufacturing Organization partnerships, how solid and transparent their Quality Management System is a deciding factor.  In this webinar, Jordi Ametller, Account Executive, and Angel Buendía, Knowledge Manager, will explore how CDMOs can stay consistently audit-ready, meet sponsor expectations, and gain a competitive edge by shifting from fragmented, manual systems to an integrated eQMS like Scilife.

     

    What you’ll learn:

    • Stay audit-ready with organized, compliant documentation.
    • Enable sponsor trust with real-time, traceable data access.
    • Close CAPAs faster with clear timelines and accountability.
    • Centralize quality control in one integrated platform.
    • Stand out to pharma clients by knowing what top CDMOs do best.