Auriga Research holds accreditations and approvals from India's leading regulatory and standards bodies, as well as international organisations including WHO and the US FDA. All 5 laboratories are NABL accredited under ISO/IEC 17025:2017 — continuously since 2003.
20+
Years NABL Accredited
5
Accredited Labs
13,216+
Accredited Test Entries
10+
Approvals & Accreditations
Our three most requested accreditation pages — each with full scope details, lab certificates, and regulatory context.
Continuously accredited since 2003 under ISO/IEC 17025:2017. 5 labs, 13,216+ test entries. Internationally recognized via ILAC & APLAC.
View full details FSSAINotified food testing laboratory at Delhi & Bangalore. Reports accepted for FSSAI licensing, import clearance, and all food categories under the FSS Act.
View full details CDSCOApproved for pharma, medical device & cosmetics testing. Reports accepted for NDAs, MDR 2017 device registrations, and import/manufacturing licences.
View full detailsEach accreditation represents a rigorous, independent assessment of Auriga's technical capability, quality systems, and regulatory compliance.
National Accreditation Board for Testing and Calibration Laboratories
India's apex body for laboratory accreditation under ISO/IEC 17025:2017. Auriga has held continuous NABL accreditation since 2003 across all 5 laboratories, with 13,216+ accredited test entries.
Central Drugs Standard Control Organisation
CDSCO-approved laboratory for pharmaceutical and medical device regulatory testing in India. Test reports accepted by state drug controllers and central licensing authorities for drug manufacturing and import licences.
Food Safety and Standards Authority of India
FSSAI-approved testing laboratory for food safety and quality analysis. Mandatory for food testing in India — results accepted for FSSAI licensing, product approvals, and regulatory submissions.
World Health Organization Prequalification Programme
WHO prequalified quality control laboratory for pharmaceutical testing. Recognized globally — essential for pharma exports and international regulatory submissions to EMEA, USFDA, and other agencies.
Bureau of Indian Standards
Recognized by the Bureau of Indian Standards for testing as per IS standards. Enables testing and certification for products requiring the BIS certification mark (ISI mark) — mandatory for many categories in India.
United States Food and Drug Administration
US FDA registered testing facility for pharmaceutical export testing. Registration enables Auriga test reports to support drug filings with the US FDA, facilitating pharma export from India to the US market.
Ministry of Ayurveda, Yoga, Naturopathy, Unani, Siddha & Homoeopathy
AYUSH-approved testing laboratory for Ayurvedic, herbal, and traditional medicine products. Enables regulatory compliance testing for Ayurvedic Drug Licence requirements under the Drugs and Cosmetics Act.
Agricultural and Processed Food Products Export Development Authority
APEDA-recognized testing laboratory for agricultural and processed food export compliance. Enables testing for export certification of agricultural commodities including fruits, vegetables, cereals, and processed foods.
International Organization for Standardization — ISO/IEC 17025:2017
Auriga Research laboratories are accredited to ISO/IEC 17025:2017 — the international standard for testing and calibration laboratory competence, jointly published by ISO and IEC.
Export Inspection Council of India
EIC-recognized laboratory for export quality certification. Enables compliance testing for agricultural and food products destined for export under the Export (Quality Control and Inspection) Act.
You can verify Auriga's accreditation status directly at nabl-india.org using the certificate numbers below.
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Test reports from Auriga are accepted by CDSCO, FSSAI, state drug controllers, US FDA, WHO, and EMA for product registration, licensing, and export compliance — without the need to repeat testing.
NABL's mutual recognition agreements with ILAC and APLAC mean Auriga results are accepted in 90+ countries. WHO Prequalification enables pharma export to markets that rely on UN procurement standards.
Accredited test reports carry the authority of an independently assessed laboratory. In disputes, recalls, or regulatory inspections, NABL-accredited reports are treated as technically sound and impartial.
Working with an accredited lab reduces the compliance burden on your QA team. Accreditation certificates demonstrate third-party verification of our quality systems — something regulators and auditors already trust.
All 5 Auriga labs are NABL accredited. Results accepted by CDSCO, FSSAI, US FDA, WHO, and 90+ countries worldwide.
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