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Liquid Chromatography Tandem Mass Spectrometry
NABL-accredited LC-MS/MS testing across 9 units in 3 labs — 250+ pesticide multi-residue analysis per FSSAI and EU MRL, ICH M7 nitrosamines (NDMA, NDEA, NMBA), mycotoxins, veterinary drug residues, PAH analysis per EC 1881/2006, and GLP bioanalytical PK/PD studies for clinical research.
Six confirmed LC-MS/MS application areas across food, pharmaceutical, environmental, herbal, and clinical research samples.
Pesticide multi-residue screening of 250+ parameters in food and agri matrices per FSSAI MRL and EU MRL limits. MRM transitions optimised for fruits, vegetables, spices, cereals, and processed foods.
Veterinary drug residue testing in food per FSSAI residue limits — antibiotics, hormones, anti-parasitics, and growth promoters in meat, milk, fish, and animal-origin products.
Multi-mycotoxin analysis in food and herbal matrices per FSSAI and EU limits — aflatoxins (B1, B2, G1, G2), ochratoxin A, fumonisins, deoxynivalenol, and zearalenone in a single LC-MS/MS run.
Nitrosamine impurity testing in pharmaceuticals per the ICH M7 genotoxic impurity framework. NDMA (AI 18 ng/day), NDEA (AI 26.5 ng/day), NMBA (AI 1.5 ng/day), and product-specific nitrosamines from risk assessments.
Polycyclic aromatic hydrocarbon (PAH) analysis in food and environmental samples per European Commission Regulation (EC) No 1881/2006 — benzo[a]pyrene and the PAH4 sum in smoked, grilled, and processed foods.
Bioanalytical method development, validation, and sample analysis for clinical PK/PD and BA/BE studies under GLP. Project-specific TAT, ICH M10 validation framework, CDSCO-aligned bioanalytical reports.
Regulatory scope note: ICH M7 (nitrosamines and genotoxic impurities) and the CDSCO 2 ppm benzene limit (residual solvent per ICH Q3C / USP 467) are distinct regulatory frameworks with different scope. Nitrosamine work falls under LC-MS/MS; residual solvent benzene per CDSCO is GC-MS scope — see GC-MS for benzene and Class 1/2/3 residual solvent quantitation.
9 LC-MS/MS units across the Delhi, Bangalore, and Manesar labs. Agilent US952 confirmed in the fleet; triple quadrupole MRM mode the default for targeted high-sensitivity analysis.
9 LC-MS/MS units distributed across the Auriga lab network supporting parallel high-throughput targeted MRM workflows for food, pharma, and bioanalytical projects.
Three LC-MS/MS units at the Delhi flagship lab supporting nitrosamine work per ICH M7, food residue testing, and pharmaceutical impurity workflows.
Three LC-MS/MS units at the Bangalore facility serving food pesticide multi-residue (250+ parameters), veterinary drug residues, and mycotoxin analysis.
One LC-MS/MS unit at the Manesar (Plot 136, Sector 5, IMT Manesar) DCGI-approved facility supporting CRD bioanalytical, PK/PD, and ICH M7 nitrosamine workflows. Remaining 2 of 9 units location to be confirmed with lab team before publishing.
Agilent US952 triple quadrupole LC-MS/MS confirmed in the platform fleet. Additional makes and models across the 9-unit fleet to be confirmed with the lab team before publishing.
Triple quadrupole tandem MS in Multiple Reaction Monitoring (MRM) mode for high-sensitivity targeted analysis. MRM provides parent-to-product ion selectivity for trace quantitation at ppb and ppt concentrations.
Six industries served by LC-MS/MS tandem mass spectrometry across the Auriga lab network.
ICH M7 nitrosamine impurity testing (NDMA, NDEA, NMBA), genotoxic impurity profiling, and trace contaminant work for CDSCO, USFDA, and EMA submissions.
View service page →250+ pesticide multi-residue, veterinary drug residues, mycotoxin panels, and PAH analysis per FSSAI MRL, EU MRL, and Codex Alimentarius limits.
View service page →PAH analysis per EC 1881/2006, trace contaminants in water, and emerging environmental pollutants requiring tandem MS sensitivity and specificity.
View service page →Mycotoxin screening (aflatoxins, OTA), pesticide residues, and trace contaminants in herbal extracts and AYUSH formulations per AYUSH and FSSAI limits.
View service page →GLP bioanalytical method development and sample analysis for PK/PD and BA/BE studies — ICH M10 validation, CDSCO-aligned reports for clinical trial submissions.
View service page →Pesticide residues, mycotoxins, and contaminant testing in dietary supplements and health products per FSSAI Health Supplements Regulations.
View service page →Three reasons pharma, food, environmental, herbal, and clinical research clients use the Auriga LC-MS/MS service.
250+ pesticides in a single analytical run. 9 LC-MS/MS units distributed across Delhi, Bangalore, and Manesar provide parallel capacity for routine and high-priority projects without queue delays.
Multiple Reaction Monitoring mode delivers trace-level detection at parts-per-billion and parts-per-trillion — the sensitivity needed for ICH M7 nitrosamines, FSSAI residue limits, and bioanalytical PK studies.
NABL-accredited LC-MS/MS reports accepted for FSSAI food submissions, CDSCO pharmaceutical filings, EU regulatory packages, and USFDA dossiers for export-bound products.
LC-MS/MS pairs with these complementary techniques across the Auriga analytical platform.
For volatile residues, residual solvents (CDSCO 2 ppm benzene per USP 467 / ICH Q3C), pesticide volatiles, and VOC analysis where the analyte is volatile or thermally stable.
View GC-MS →For elemental contaminants — ICH Q3D(R2) heavy metals, FSSAI food heavy metals, and IS 10500 water trace metals complementing LC-MS/MS organic impurity work.
View ICP-MS →9 LC-MS/MS units across Delhi, Bangalore, and Manesar. 250+ pesticides in a single run, ICH M7 nitrosamines, FSSAI mycotoxins, and GLP bioanalytical work. Standard TAT 5 to 7 working days.
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