cGMP Compliance Solutions

End-to-End cGMP
Services & Support

From initial inspection through certification, ongoing audits, and compliant software — NPGMA delivers the expertise and tools your facility needs to achieve and maintain cGMP compliance with confidence.

6
Core Service Areas
FDA
Regulation Aligned
Non-Profit
Independent Organization

What We Offer

Our cGMP Service Portfolio

Comprehensive compliance services tailored for food, dietary supplement, cosmetic, and natural product manufacturers at every stage of the certification journey.

Inspection

cGMP Inspection

Thorough facility inspections conducted by NPGMA-credentialed assessors to evaluate your manufacturing environment, processes, and documentation against current Good Manufacturing Practice regulations.

  • Pre-inspection readiness review
  • On-site facility walk-through
  • Documentation & record review
  • Detailed findings report with prioritized gaps
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Core Service

cGMP Certification

NPGMA's accredited certification program provides independent, third-party verification that your facility operates in full compliance with FDA cGMP regulations — giving customers and regulators confidence in your products.

  • Accredited third-party certification
  • FDA-aligned evaluation criteria
  • Official NPGMA certificate & seal
  • Publicly verifiable on npgma.org
Start your application
Ongoing Compliance

cGMP Auditing

Scheduled and unannounced audit services to ensure your facility maintains cGMP compliance between certification cycles. Identify vulnerabilities before regulators do.

  • Annual & periodic surveillance audits
  • Supplier / contract manufacturer audits
  • Mock FDA inspection preparation
  • CAPA development & tracking support
Schedule an audit
Education

cGMP Training Materials

Professionally developed training resources that equip your workforce with the cGMP knowledge they need — from production floor staff to quality management teams.

  • Role-specific training modules
  • Visual SOPs & quick-reference guides
  • Competency assessments & sign-off records
  • New-hire onboarding curriculum
Request materials
Documentation

SOP Creation

Custom Standard Operating Procedures drafted by cGMP compliance specialists — written to FDA standards, tailored to your specific facility, equipment, and product categories.

  • Facility- and process-specific drafting
  • Master SOP library development
  • Version control & revision history built in
  • Review, approval & training workflows
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Technology

cGMP Compliant Software Modules

Purpose-built software modules designed to digitize, streamline, and enforce cGMP compliance across your facility's critical quality systems — reducing paper burden, human error, and audit risk.

Master Batch Records (MBR) Electronic Batch Records SOP Management Compliant Document Storage CAPA Tracking Training Record Management Audit Trail Logs Change Control
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How It Works

Your Path to cGMP Certification

1

Initial Assessment

We evaluate your current facility, processes, and documentation to identify gaps against cGMP standards.

2

Remediation & Training

SOPs are developed or updated, staff are trained, and compliant systems are put in place.

3

Formal Audit

An NPGMA auditor conducts a comprehensive on-site review against FDA cGMP requirements.

4

Certification Issued

Upon passing, your facility receives the official NPGMA cGMP Certified seal, publicly verifiable online.

Independent & Non-Profit

NPGMA is an independent not-for-profit organization with no commercial ties — our certifications are objective and trustworthy.

Publicly Verifiable

Every NPGMA certificate can be verified instantly at npgma.org — giving buyers and regulators real-time confirmation of your status.

Expert Assessors

Our auditors bring deep industry experience in food, dietary supplements, cosmetics, and natural product manufacturing.

Ready to get started?

Contact NPGMA today to discuss which services best fit your facility's needs — from a single inspection to a full compliance program.

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Training

Good Manufacturing Practices Internet Course

This Good Manufacturing Practices (GMP) Internet course is designed to review the requirements of Part 110 – Current Good Manufacturing Practices in the Manufacturing, Packing, or Holding of Human Food – in Title 21 of the U.S. Code of Federal Regulations.

  • Covers basic sanitary controls for FDA regulated food operations
  • Relevant for food processors, wholesalers, distributors, warehouses, and storage facilities
  • Designed for supervisors, middle managers, and quality control personnel
  • Supports teams responsible for meeting current GMP requirements