Skip to main content

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?

  • Going beyond minimum requirements

  • Maintaining high standards every day—not just during audits

  • Creating a culture where food safety and hygiene are priorities

  • Ensuring consistency, traceability, and risk management across operations

Signs Your Facility Is Just Barely Passing Audits

  • Cleaning schedules are updated only before an audit

  • Staff only follow hygiene practices when auditors are present

  • Documentation is rushed or backdated

  • No regular internal audits or follow-ups

  • Corrective actions are reactive, not preventive

  • GMP training is outdated or not site-specific

  • External audit prep is done in panic mode

Traits of a Truly GMP-Compliant Facility

1. Cleanliness and Sanitation Are Daily Priorities

  • Cleaning SOPs are followed and verified daily

  • Sanitation records are complete, consistent, and real-time

  • Equipment is maintained in hygienic, food-safe condition

2. Consistent Staff Behavior

  • Handwashing, PPE, and hygiene rules are second nature

  • Staff take ownership of food safety and cleanliness

  • Training is refreshed regularly and applied practically

3. Documentation Is Timely and Accurate

  • Records are filled out during operations, not post-shift

  • Procedures are followed as written, not “adjusted” during work

  • Documentation is reviewed and verified periodically

4. Equipment and Facility Are Maintained Proactively

  • Preventive maintenance is scheduled and tracked

  • Facility structure supports hygienic design and zoning

  • Pest control is monitored and reviewed monthly

5. Internal Audits Are Regular and Objective

  • Monthly or quarterly GMP self-inspections

  • Audit findings lead to real corrective actions

  • Trends and recurring issues are addressed systemically

6. Suppliers and Raw Materials Are Controlled

  • Suppliers are GMP-audited or qualified

  • Incoming goods checks are standardized

  • Storage conditions are monitored and recorded

7. Management Is Actively Involved

  • Leadership conducts routine GMP walkthroughs

  • Management supports a food safety culture

  • Resources are allocated for training, tools, and improvements

Why It Matters

  • True compliance reduces product recalls and contamination risks

  • Builds customer trust and improves brand reputation

  • Strengthens readiness for customer, regulatory, and certification audits

  • 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.

Leave a Reply