
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.
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.
National Safety Foundation cGMP certification validates that our manufacturing processes, facilities, and quality systems meet the highest industry standards for dietary supplement manufacturing.
Our quality management system is certified to ISO 9001:2015, demonstrating our commitment to consistent quality, continuous improvement, and customer satisfaction across all operations.
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.
All products are manufactured in compliance with the quality standards of the United States Pharmacopeia (USP), ensuring consistent potency, purity, and quality.
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 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.

Every incoming raw material is tested in our ISO/IEC 17025 accredited lab before entering production. Identity, potency, and purity verified.
Continuous monitoring and documentation throughout manufacturing. Real-time process control at every critical control point.
Every batch undergoes comprehensive finished product testing before release. Certificate of Analysis (COA) issued for every lot.
Accelerated and real-time stability studies to confirm shelf life and potency claims throughout the product's lifecycle.
Complete batch records, SOPs, and traceability from raw material to finished product. Full audit trail maintained.
CAPA system, internal audits, and management review processes ensure continuous improvement of our quality systems.
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.
Testing support and quality documentation workflows for brands requiring COAs, ingredient verification, batch review, and compliance-focused product documentation.
Request Testing SupportManufacturing and quality support for compliant hemp-derived product concepts, with pharmaceutical-style documentation, traceability, testing, and quality protocols where applicable.
Discuss Hemp Manufacturing SupportProduct development support for new supplement concepts, ingredient combinations, delivery formats, flavor direction, and formulation refinement.
Develop a New FormulaSupport for supplement brands, distributors, clinics, retailers, and entrepreneurs seeking ready-to-launch or customized supplement product lines.
Start a Supplement LineWe provide full cGMP documentation, batch records, and COAs for all manufacturing projects. Contact us to request our quality documentation package.