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US Pharma Lab’s group of companies are locally and globally certified to be in compliance with all relevant quality norms. All facilities in the United States, India, and China have been FDA audited and NSF certified for cGMP compliance. Additionally, the global facilities follows strict Allergen Control and HACCP Plans, Foreign Material Control, and Dietary Supplement 21 CFR Part 111 Protocols.

In addition, US Pharma Lab India is ISO9001, FSSAI, and WHO GMP certified. Inspections for compliance are performed by third-party agencies based out of Europe, Australia, Asia, and Africa.

The company’s in-house QA/QC department is operated by a team of accredited scientists who pride themselves on adhering and complying with a list of international quality standards:

US FDA (US Food and Drug Administration)
NSF GMP (NSF accredited for cGMP compliance
Dietary Supplement 21 CFR part 111 Compliance
NABL (National Accreditation Board of Testing & Calibration Laboratories)
DCGI (Department of Ayurveda, Yoga and Naturopathy, Unani, Siddha, and Homeopathy)
GLP (Good Laboratory Practices)
WHO GMP (World Health Organization Good Manufacturing Practices)
ISO 9001:2008 (International Organization for Standardization)
ISO/IEC 17025:2005 (International Organization for Standardization)
ISO 14001 (International Organization for Standardization)
ISO 18001 (International Organization for Standardization)
FSSAI (Food Safety and Standards Authority of India)

The fully equipped and modern laboratories offer quantification of dietary supplements as well as:

Vitamin and amino analysis on HPLC
Mineral analysis on ICP-OES, On ICP-MS
Botanical identification/standardization – HPLC, GC, UV
Endotoxin testing – LAL method
Heavy Metal analysis on ICP-MS
Testing of Aflatoxins – B1, B2, GI and G2 by HPLC
Pesticides residue analysis – USP, AOAC, EPA on GC and HPLC
Microbiological contamination testing
Irradiation and radioactive testing on PSL
Residual solvent analysis according to ICH guidelines – Q3 on GC

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