In regulated pharma and CDMO environments, GMP compliance isn’t just about systems—it’s about culture. This webinar, hosted by Blue Mountain with guest speaker Shane McGrath, Validation Manager at Corium Innovations, explores how life sciences organizations can achieve, sustain, and elevate compliance while embracing digital transformation.
You’ll hear how Corium transitioned from Blue Mountain’s legacy Calman to RAM R4 during a period of COVID-driven change, and how they overcame challenges like underutilized system capabilities, cultural resistance, and process redesign. Key takeaways include:
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How enterprise asset management (EAM) unifies maintenance, calibration, validation, and inventory for GMP compliance
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Practical steps for mapping processes before digitalization to avoid replicating inefficiencies
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Strategies for change management, staff training, and role-based adoption
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Real-world results, including a 20% increase in on-time maintenance completion within one year
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The importance of vendor partnership and scalability in long-term compliance success
Watch the replay to learn how thoughtful digitalization can deliver audit-ready operations, efficiency gains, empowered teams, and a stronger culture of compliance.