Quality & Compliance
Quality & Compliance

Five certifications. One uncompromising standard.

Our quality systems are not just compliant — they are accredited, audited, and continuously improved. Every batch is tested. Every process is documented. Every product is released with a Certificate of Analysis.

Our Credentials

Certifications that prove our commitment.

FDA

FDA Registered Facility

FDA 21 CFR 111

Pharma Natural is licensed and registered with the Food and Drug Administration (FDA). Since inception, the company has operated in compliance with FDA 21 CFR 111 — Current Good Manufacturing Practice for dietary supplements.

NSF

NSF cGMP Certified

NSF/ANSI 173

National Safety Foundation cGMP certification validates that our manufacturing processes, facilities, and quality systems meet the highest industry standards for dietary supplement manufacturing.

ISO

ISO 9001 Certified

ISO 9001:2015

Our quality management system is certified to ISO 9001:2015, demonstrating our commitment to consistent quality, continuous improvement, and customer satisfaction across all operations.

17025

ISO/IEC 17025:2017 Accredited

ISO/IEC 17025:2017

Our in-house testing laboratory is accredited to ISO/IEC 17025:2017 — the international standard for testing and calibration laboratories. This means our QC results are internationally recognized and technically competent.

USP

USP Quality Standards

United States Pharmacopeia

All products are manufactured in compliance with the quality standards of the United States Pharmacopeia (USP), ensuring consistent potency, purity, and quality.

WBE

WBENC Certified

Women's Business Enterprise

Pharma Natural is certified by the Women's Business Enterprise National Council (WBENC), recognizing our status as a women-owned business enterprise.

ISO/IEC 17025:2017

Internationally accredited in-house testing laboratory.

ISO/IEC 17025:2017 is the international standard that specifies the general requirements for the competence, impartiality, and consistent operation of testing and calibration laboratories. Accreditation to this standard means our test results are internationally recognized.

Our accredited laboratory tests raw materials and finished products for identity, potency, purity, and contaminants. This in-house capability means faster release times, lower costs, and complete control over quality data.

Identity Testing
Potency Verification
Purity Analysis
Contaminant Screening
Microbiological Testing
Heavy Metal Analysis
Dissolution Testing
Stability Studies
ISO 17025 accredited laboratory
Quality Control Process

From raw material to finished product — every step tested.

01

Raw Material Testing

Every incoming raw material is tested in our ISO/IEC 17025 accredited lab before entering production. Identity, potency, and purity verified.

02

In-Process Controls

Continuous monitoring and documentation throughout manufacturing. Real-time process control at every critical control point.

03

Finished Product Testing

Every batch undergoes comprehensive finished product testing before release. Certificate of Analysis (COA) issued for every lot.

04

Stability Testing

Accelerated and real-time stability studies to confirm shelf life and potency claims throughout the product's lifecycle.

05

Documentation & Traceability

Complete batch records, SOPs, and traceability from raw material to finished product. Full audit trail maintained.

06

Continuous Improvement

CAPA system, internal audits, and management review processes ensure continuous improvement of our quality systems.

Our Facility

State-of-the-science. Miami Lakes, Florida.

Pharma Natural's base of operations is in a state-of-the-science manufacturing facility in the prestigious Miami Lakes Research & Industrial Park in Miami Lakes, Florida.

Our facility is designed for pharmaceutical-grade manufacturing with full environmental controls, documented cleaning procedures, and equipment qualification protocols.

Health Sciences & R&D Lab
ISO/IEC 17025 QC Lab
Manufacturing Floor
Packaging Operations
Climate-Controlled Warehouse
Client Services Office
24+
Years FDA Registered
8
Major Certifications
300+
Proven Formulations
100%
Batch COA Coverage
Partnership Programs

Quality Systems That Support Commercial Growth

Quality & Testing

Third-Party Lab Testing Coordination

Testing support and quality documentation workflows for brands requiring COAs, ingredient verification, batch review, and compliance-focused product documentation.

Request Testing Support
CBD / Hemp Quality Protocols

Hemp-Derived Product Manufacturing Support

Manufacturing and quality support for compliant hemp-derived product concepts, with pharmaceutical-style documentation, traceability, testing, and quality protocols where applicable.

Discuss Hemp Manufacturing Support
R&D Capability

In-House Research & Formulation Development

Product development support for new supplement concepts, ingredient combinations, delivery formats, flavor direction, and formulation refinement.

Develop a New Formula
Core Manufacturing Revenue Channel

Private Label & White Label Supplements

Support for supplement brands, distributors, clinics, retailers, and entrepreneurs seeking ready-to-launch or customized supplement product lines.

Start a Supplement Line
Partner With Confidence

Request our quality documentation package.

We provide full cGMP documentation, batch records, and COAs for all manufacturing projects. Contact us to request our quality documentation package.