What We Test

Auriga Research operates across eight testing verticals with over 5,000 test parameters under NABL accreditation. Below is a summary of what we test — and, equally important, what we currently do not offer. Transparency builds trust.

Our Testing Services

Pharmaceutical Testing

  • Dissolution Testing
  • Stability Studies (ICH)
  • Impurity Profiling
  • Method Development & Validation
  • Raw Material Testing
  • Finished Product Analysis
  • Bioanalytical Studies
  • Extractable & Leachable Studies
View all pharmaceutical testing services

Food Testing

  • Nutritional Analysis & Labelling
  • Microbiological Testing
  • Pesticide Residue Analysis
  • Heavy Metals Testing
  • Adulterant Detection
  • Allergen Testing
  • Shelf Life Studies
  • FSSAI Compliance Testing
View all food testing services

Water Testing

  • Drinking Water (IS 10500)
  • Packaged Water (IS 14543)
  • Wastewater / Effluent
  • Swimming Pool Water
  • Boiler & Cooling Water
  • Groundwater Analysis
View all water testing services

Environmental Testing

  • Air Quality Monitoring (Ambient & Stack)
  • Soil Testing
  • Noise Level Assessment
  • Waste Characterisation
  • EIA Studies Support
  • CPCB/SPCB Compliance
View all environmental testing services

Clinical Trials

  • Bioequivalence Studies
  • Bioavailability Studies
  • Phase I-IV Clinical Trials
  • BA/BE Analytical Support
  • Clinical Sample Analysis
View all clinical trials services

Cosmetics & Personal Care

  • Stability Testing
  • Preservative Efficacy (PET)
  • Heavy Metals & Microbial Limits
  • Claims Substantiation
  • BIS Compliance (IS 4707 / IS 4011)
  • Dermal Safety Assessment
View all cosmetics & personal care services

Nutraceutical Testing

  • Active Ingredient Assay
  • Disintegration & Dissolution
  • Heavy Metals & Pesticide Residues
  • Microbial Limits
  • Stability Studies
  • Label Claim Verification
View all nutraceutical testing services

Medical Device Testing

  • Biocompatibility (ISO 10993)
  • Chemical Characterisation
  • Sterility Testing
  • Endotoxin Testing (LAL)
  • Extractable & Leachable
  • Shelf Life / Ageing Studies
View all medical device testing services

Not Sure Which Tests You Need?

Describe your product and regulatory goal. Our technical team will recommend the right testing scope within 4 business hours.

+91-7428116100 Request a Quote

What We Currently Don't Offer

We believe in being upfront about our scope. The following tests are outside our current capabilities. If you need any of these, we can recommend trusted partner laboratories.

SPF 50+ In-Vivo Testing

In-vivo SPF testing on human subjects requires specialized clinical dermatology facilities. We offer in-vitro SPF testing up to SPF 30.

Microplastics Analysis

Dedicated microplastics quantification by FTIR/Raman microscopy is not currently in our scope. We are evaluating instrumentation for future capability.

NMR Spectroscopy

We do not operate nuclear magnetic resonance instruments. For structural elucidation requiring NMR, we can recommend partner laboratories.

Zetasizer / Dynamic Light Scattering

Particle size analysis by DLS/Zetasizer is not currently available. We offer laser diffraction-based particle size analysis.

Full Bioequivalence Studies (in-house)

Clinical bioequivalence studies are conducted through our clinical division partner. Bioanalytical support (sample analysis) is performed in-house.

Sensory Panel Evaluation

Trained sensory panel testing for taste, texture, and aroma profiling is not part of our current service offering.

This list is updated periodically as we expand capabilities. If you need a test not listed above, submit a request and our team will assess whether we can accommodate it or recommend an alternative.

Frequently Asked Questions

How do I check if you can test my specific product?
The fastest way is to submit a quote request with your product details and required parameters. Our technical team evaluates feasibility within 4 business hours and responds with confirmation, pricing, and turnaround time. You can also call us at +91-7428116100 for immediate guidance.
Can you develop new test methods for non-standard parameters?
Yes. Our method development and validation team can develop and validate analytical methods for non-pharmacopoeial or non-standard parameters. This includes method development by HPLC, GC, LC-MS/MS, ICP-MS, and other techniques. Method development timelines and costs are quoted separately based on complexity.
Do you test as per international standards (USP, BP, EP)?
Yes. Our pharmaceutical testing is performed per Indian Pharmacopoeia (IP), United States Pharmacopeia (USP), British Pharmacopoeia (BP), European Pharmacopoeia (EP), and Japanese Pharmacopoeia (JP) methods. For food and water, we follow FSSAI, BIS, AOAC, ISO, and Codex methods.
Are your test reports accepted for regulatory submissions?
Yes. Our NABL-accredited test reports are accepted by CDSCO, FSSAI, BIS, CPCB/SPCB, and state drug controllers for regulatory filings. For international submissions, our reports are accepted by USFDA, WHO, and other regulatory bodies based on our accreditation scope.

Ready to Start Testing?

Send us your product details and we will confirm scope, pricing, and timeline.

+91-7428116100 Get a Free Quote

Type to search services, tests, and locations…