Program Overview
The NPGMA GMP Certification Program verifies that member suppliers' manufacturing practices conform to standardized good manufacturing practices. Certification is based on comprehensive third-party inspections and documentation reviews to ensure compliance with established quality standards, including identity, purity, strength, and composition.
Certification Eligibility
Suppliers achieving an “A” compliance rating during an NPGMA GMP audit qualify for certification and may display the NPGMA GMP certification seal. This certification demonstrates adherence to recognized manufacturing practices and represents facility and process certification rather than individual product certification.
Maintaining Certification
Certified companies must remain active NPGMA members, comply with GMP standards, meet supplier membership requirements, pay annual certification fees, and undergo re-audits every two years.
Program Oversight
A GMP Advisory Committee composed of industry experts provides guidance and oversight. Members represent diverse sectors including food, dietary supplements, pharmaceuticals, and botanicals.
Auditor Qualifications
NPGMA auditors are selected based on their qualifications and experience in conducting inspections of food and dietary supplement manufacturers. They are trained in NPGMA GMP standards and performance rating systems.
On-Site Audit Process
On-site audits verify compliance with NPGMA GMP standards. Facilities involved in manufacturing, packaging, labeling, testing, holding, and distribution are inspected to ensure that processes are controlled and meet established specifications for quality.
Interested in NPGMA GMP Certification?
Contact NPGMA to learn more about certification requirements, audit procedures, and how your organization can become GMP certified.
Request Information