CGMP Compliance Documentation & Training Bundle
FDA CGMP SOP Templates & Training for Food Manufacturing Facilities (21 CFR 117 Subpart B)
The CGMP Compliance Documentation & Training Bundle provides a comprehensive, FDA-aligned system with ready-to-use SOP templates, policies, forms, records, and employee training materials to support compliance with 21 CFR Part 117 Subpart B (CGMPs), enabling food manufacturers, processors, packers, and holding facilities to achieve audit readiness, FDA inspection preparedness, and operational standardization through a complete compliance framework without building documentation from scratch.
What’s Included in the CGMP Compliance Bundle
Programs & Policies
- • CGMP Compliance Policy
- • Personnel Hygiene and Health Program
- • Facility Sanitation Policy
- • Equipment & Utensil Control Program
- • Pest Control Policy
- • Plant Design and Maintenance Policy
- • Product Holding, Storage, and Distribution Policy
- • Defect Action Level Management Policy
- • FDA CGMP program implementation
- • Facility-wide sanitation and hygiene control
- • Preventive operational compliance
- • Audit-ready policy documentation
Procedures (SOPs)
- • Hand Washing SOP
- • Sanitary Facility Maintenance SOP
- • Pest Prevention & Control SOP
- • Sanitation SOP for Food Contact Surfaces
- • Waste and Offal Disposal SOP
- • Equipment Cleaning & Maintenance SOP
- • Ice Use & Water Source Control SOP
- • Environmental Monitoring SOP
- • Non-Food Contact Cleaning SOP
- • Allergen Cross-Contact Prevention SOP
- • FDA sanitation and hygiene compliance
- • Cross-contamination and allergen control
- • Environmental and operational monitoring
- • Standardized cleaning and maintenance procedures
Forms & Records
- • Daily Personnel Hygiene Checklist
- • Sanitation Log (Food & Non-Food Contact Surfaces)
- • Pest Control Log
- • Equipment Cleaning & Maintenance Log
- • Storage Temperature Monitoring Log
- • Employee Illness Reporting Form
- • Water Quality Monitoring Form
- • Facility Inspection Checklist
- • Corrective Action & Deviation Report
- • Waste Disposal Tracking Log
- • FDA-required recordkeeping
- • Real-time monitoring and verification
- • Inspection and audit documentation
- • Corrective action tracking and compliance evidence
- • Daily Personnel Hygiene Checklist
- • Sanitation Log (Food & Non-Food Contact)
- • Pest Control Log
- • Equipment Cleaning & Maintenance Log
- • Storage Temperature Monitoring Log
- • Employee Illness Reporting Form
- • Water Quality Monitoring Form
- • Facility Inspection Checklist
- • Corrective Action & Deviation Report
- • Waste Disposal Tracking Log
Training Materials
- • Slide Deck: Introduction to 21 CFR 117 Subpart B
- • Job Aid: CGMP Do’s and Don’ts
- • Employee Cleanliness & Sanitation Quiz
- • Food Contact Surface Cleaning Quick Guide
- • Trainer’s Guide for Supervisors
- • Certificate of Completion Template
- • Annual Refresher Training Module
- • Employee CGMP training requirements
- • Workforce hygiene and sanitation awareness
- • Supervisor-led training implementation
- • Ongoing compliance through refresher programs
Who This CGMP Bundle Is For
- • Food manufacturers, processors, and packing facilities
- • Warehousing and distribution operations handling food products
- • Compliance managers and QA professionals
- • Facilities preparing for FDA inspections or third-party audits
- • Companies aligning with GFSI schemes (SQF, BRCGS, FSSC 22000)
Why This CGMP Bundle Matters
- • Built specifically for 21 CFR 117 Subpart B compliance
- • Covers policies, SOPs, records, and training in one system
- • Supports FDA inspections, internal audits, and certification readiness
- • Eliminates the need to develop documentation internally
- • Scalable for facility size, product type, and operational complexity
Access & Implementation
- • Access is tailored based on: Facility type and operational scope
- • Product category and risk level
- • Level of support required (self-implementation or advisory support)
Optional Add-On Services
- - Conducted remotely to assess facility compliance against 21 CFR 117 Subpart B requirements.
- - Comprehensive in-person evaluation of CGMP compliance and facility conditions.
- - Translation of SOPs and training materials into Spanish, French, or other required languages.
- - Enhancement and crosswalk of CGMP documentation to meet GFSI certification requirements.
Get Started with CGMP Compliance Documentation
This bundle provides a ready-to-use, FDA-aligned compliance framework covering:
- • Sanitation and hygiene programs
- • Operational control procedures
- • Monitoring logs and compliance records
- • Employee training and competency programs
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