Introduction: What is GMP Auditing?
GMP (Good Manufacturing Practices) are essential standards required in the food, pharmaceutical, cosmetic, and medical device sectors to ensure product safety and quality.
GMP Auditing is the systematic examination of procedures, personnel, equipment, and documentation to verify that they conform to GMP standards—especially in food production and processing.
For food manufacturing consultants and safety officers, GMP audits serve as a critical control mechanism for risk management and regulatory compliance.
1. Purpose and Importance of GMP Auditing
GMP audits help to:
- Identify gaps in hygiene, sanitation, and documentation
- Reduce contamination risks
- Ensure regulatory and customer compliance
- Promote a culture of food safety and accountability
Audits must be thorough, and all staff involved in production should maintain evidence of compliance with food safety protocols and SOPs.
2. Role of GMP Auditing in Daily Operations
Key GMP practices that auditors check include:
2.1 Employee Hygiene and Training
- Proper clothing and PPE (no jewelry or loose garments)
- No food, smoking, or unauthorized materials in production areas
- Verified food safety training and education
2.2 Ground and Facility Maintenance
- Waste treatment and drainage systems
- Cleanliness of surroundings and pest control
2.3 In-Plant Sanitation
- Controlled chemical storage and proper handwashing facilities
- Measures for pest prevention and sanitation
2.4 Equipment and Processing Zones
- Clean and food-grade equipment to avoid contamination
- Maintenance logs and cleaning validation reports
2.5 Warehouse and Distribution
- Well-sanitized, temperature-controlled storage
- Traceability of inbound and outbound products
3. Types of GMP Audits
There are three types of audits in the food and beverage industry:
3.1 First Party Audit (Internal)
- Conducted by the company’s own staff or hired consultants
- Ensures internal compliance before external scrutiny
3.2 Second Party Audit
- Conducted by a customer to verify their supplier’s quality and GMP compliance
- Useful when third-party certifications don’t fully cover custom requirements
3.3 Third Party Audit
- Carried out by certification bodies like ISO, BRCGS, or SQF
- Leads to formal certifications like ISO 22000, HACCP, or ISO 9001
A qualified food business consultancy can help prepare facilities for all three audit types through mock audits, CAPA planning, and SOP development.
4. Common GMP Certifications for Food Industry
To comply with global food safety expectations, the following certifications are commonly required:
- HACCP (Hazard Analysis and Critical Control Points)
- ISO 22000 (Food Safety Management System)
- SQF (Safe Quality Food Program)
- ISO 9001 (Quality Management System)
These certifications provide structured frameworks for safe food production, record keeping, and personnel hygiene.
5. GMP Audit Checklist: Key Focus Areas
A typical GMP audit includes checks in the following seven categories:
- Buildings and Facilities
- Equipment and Utensils
- Production and Process Control
- Packaging and Labelling
- Warehouse and Distribution
- Documentation and Records
- Organizing and Personnel
Each element is evaluated against defined GMP standards and regulatory requirements.
6. Conclusion: Why GMP Audits Are Non-Negotiable
GMP auditing is not just a compliance requirement—it’s an operational safeguard. It ensures that food products are safe, consistent, and fit for consumption.
By implementing GMP audits regularly, companies can:
- Enhance product quality
- Minimize recall risks
- Meet customer and export market expectations
- Foster a culture of accountability and hygiene
If you're setting up or improving a food manufacturing unit, working with a professional food consultant or food processing consultant ensures readiness for audits, certifications, and long-term success.