Master QMS Implementation in Life Sciences
Transform Your Quality Management Today
Are you among the 71% of life sciences companies struggling with partial quality management system (QMS) implementation? Our industry brief reveals how leading organisations have overcome common implementation challenges to fully digitise their quality processes. Discover the three vital implementation steps that will help you maximise QMS software ROI and achieve quality excellence across all facilities.
- Learn proven strategies for aligning stakeholders and resources to ensure successful QMS implementation.
- Discover configuration best practices that reduce validation time from months to hours.
- Understand how to minimise disruption during go-live and gain employee buy-in for your life science QMS.
Trusted By These Life Science Leaders
Paper holds you back. Digital propels you forward.
Despite 85% of life sciences companies purchasing quality management systems, only 29% have fully implemented them across all facilities. This implementation gap creates real challenges, as proven by the fact that 32% of quality professionals report major issues with paper-based processes.
Why stay stuck? By fully digitising quality processes, you'll gain competitive advantages through streamlined workflows and faster time-to-market. The right QMS software connects document management, training, quality events, and audits in one system. You'll create a single source of truth for your global operations.
Companies that overcome implementation barriers don't just improve efficiency—they transform how they deliver life-changing products to patients. Isn't that why you got into this business in the first place?
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Common Questions on QMS Implementation in Life Sciences
What blocks successful QMS implementation?
The top three barriers are cost justification (46%), transition time (39%), and concerns about business disruption (33%). With strategic planning, you can address these challenges and move forward with confidence.
How can we reduce validation burden?
Modern QMS solutions offer risk-based validation tools that align with U.S. Food and Drug Administration (FDA) guidance. Focus your efforts where they matter most and cut validation time from months to 20 hours or less.
Which quality processes should be digital?
Document management, training, quality events, and audits are critical to digitise. When these systems operate together, you'll achieve greater efficiency and stay audit-ready.
How do we ensure employee adoption?
Download the brief to learn how to involve key stakeholders early, communicate benefits clearly, and leverage vendor training. The right tools will automate procedure creation and role assignment to minimise resistance.
Transform Your Life Sciences Quality Operations
Ready to implement your QMS the right way? We'll show you how.
Get Your Implementation GuideMasterControl Solutions for Life Sciences
We've helped hundreds of life sciences organisations implement QMS solutions that actually get used across all facilities.
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Validation Tool
Cut validation time to hours or minutes—not days—using our patented Validation Excellence Tool (VxT).
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Rapid Onboarder
Reduce data onboarding time by an average of 57% through automated aggregation and loading.
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Operations Tool
Create procedures and work instructions in hours instead of weeks with our Operations Procedure Builder.
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Global Visibility
Standardise quality processes across all facilities with a single source of truth for worldwide operations.
