Is Your Facility Truly GMP Compliant or Just Barely Passing Audits?
Good Manufacturing Practices (GMP) are the foundation of safe, high-quality food and pharmaceutical production. But there’s a big difference between barely passing a GMP audit and truly being compliant every day. Is your facility just ticking boxes—or genuinely protecting consumers and your brand?
What Does “Truly GMP Compliant” Mean?
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Going beyond minimum requirements
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Maintaining high standards every day—not just during audits
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Creating a culture where food safety and hygiene are priorities
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Ensuring consistency, traceability, and risk management across operations
Signs Your Facility Is Just Barely Passing Audits
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Cleaning schedules are updated only before an audit
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Staff only follow hygiene practices when auditors are present
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Documentation is rushed or backdated
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No regular internal audits or follow-ups
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Corrective actions are reactive, not preventive
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GMP training is outdated or not site-specific
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External audit prep is done in panic mode
Traits of a Truly GMP-Compliant Facility
1. Cleanliness and Sanitation Are Daily Priorities
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Cleaning SOPs are followed and verified daily
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Sanitation records are complete, consistent, and real-time
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Equipment is maintained in hygienic, food-safe condition
2. Consistent Staff Behavior
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Handwashing, PPE, and hygiene rules are second nature
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Staff take ownership of food safety and cleanliness
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Training is refreshed regularly and applied practically
3. Documentation Is Timely and Accurate
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Records are filled out during operations, not post-shift
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Procedures are followed as written, not “adjusted” during work
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Documentation is reviewed and verified periodically
4. Equipment and Facility Are Maintained Proactively
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Preventive maintenance is scheduled and tracked
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Facility structure supports hygienic design and zoning
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Pest control is monitored and reviewed monthly
5. Internal Audits Are Regular and Objective
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Monthly or quarterly GMP self-inspections
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Audit findings lead to real corrective actions
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Trends and recurring issues are addressed systemically
6. Suppliers and Raw Materials Are Controlled
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Suppliers are GMP-audited or qualified
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Incoming goods checks are standardized
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Storage conditions are monitored and recorded
7. Management Is Actively Involved
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Leadership conducts routine GMP walkthroughs
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Management supports a food safety culture
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Resources are allocated for training, tools, and improvements
Why It Matters
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True compliance reduces product recalls and contamination risks
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Builds customer trust and improves brand reputation
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Strengthens readiness for customer, regulatory, and certification audits
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Ensures compliance with ISO 22000, HACCP, and FSSC 22000
CAYS Scientific Helps You Go Beyond Bare Minimum
At CAYS Scientific, we help you:
✅ Conduct in-depth GMP audits and gap analysis
✅ Provide tailored staff training and SOP improvement
✅ Strengthen documentation and hygiene monitoring
✅ Establish sustainable compliance—not just audit survival
📞 Contact CAYS Scientific today to upgrade your GMP practices from “just passing” to industry leading.