NABL · ISO 17025 · USFDA · WHO PQ · NAFDAC

International Testing Services India: ISO 17025, USFDA and WHO PQ Accepted Reports

Export with Confidence.

Auriga Research works with clients in over 30 countries, providing NABL-accredited ISO/IEC 17025 compliant test reports accepted by FDA, WHO, EMA, and NAFDAC Nigeria. USD-priced testing is available with chain-of-custody sample import logistics and dedicated international account management across pharma, nutraceuticals, cosmetics, food, medical devices, and consumer products.

Backed by the Arbro Group's analytical heritage, with Arbro Lab operational since 1990 and Auriga Research founded in 2007, the group has held NABL accreditation continuously since 2003 without a single break.

Choose Your Path

International clients fall into two distinct groups, each with its own regulatory framework and report expectations. Pick the path that fits your scope.

International Pharma & Biotech Clients

Pharmaceutical and biotech sponsors needing analytical testing for FDA, EMA, and WHO Prequalification submissions, with ISO/IEC 17025 analytical scope.

  • FDA (ANDA, NDA, 510(k))
  • EMA Marketing Authorisation
  • WHO Prequalification
  • ISO/IEC 17025 analytical scope
  • 21 CFR Part 11 audit-trail data
Discuss Dossier Testing

International Food, Agri & Consumer Goods Clients

Food, agri-commodity, cosmetics, and consumer goods importers needing pre-export and destination-market compliance certificates from an Indian NABL lab.

  • APEDA and EIC export credentials
  • EU MRL (Regulation EC 396/2005)
  • Japan Positive List residues
  • Codex Alimentarius limits
  • NAFDAC Nigeria and GCC frameworks
Discuss Export Testing

Who Needs This

Six international buyer profiles use Auriga's testing service across pharma, nutraceuticals, cosmetics, medical devices, food and agri, and multinational market-entry programmes.

International Pharmaceutical & Biotech

Pharmaceutical and biotech sponsors sourcing analytical testing for ANDA, NDA, EMA, or WHO PQ dossiers, including stability, impurity profile, and method validation work.

International Nutraceutical Brands

Nutraceutical, supplement, vitamin, and functional food brands manufactured or sourced in India needing destination-market analytical packages.

International Cosmetics & Personal Care

Cosmetics, skincare, and personal care brands testing products manufactured or sourced in India, including safety, stability, and claim substantiation evidence.

International Medical Device Manufacturers

Medical device manufacturers building ISO 10993 technical files for FDA 510(k), EU MDR, and CDSCO submissions.

Overseas Food, Agri & Consumer Goods Importers

Food, agri-commodity, consumer product, and packaging importers needing pre-export compliance certificates from an Indian NABL-accredited laboratory.

Multinational Companies Entering India

Multinationals needing India-specific regulatory compliance before market entry, including BIS, FSSAI, CDSCO, AYUSH, and environmental product panels.

Why Auriga

Six reasons international clients choose Auriga as their Indian testing partner.

Reports Accepted in 30+ Countries

Reports are accepted by regulatory authorities and buyers across the EU, US, UK, GCC, Japan, ASEAN, Africa, and other markets, supported by NABL ILAC mutual recognition.

US FDA Registered and WHO Prequalified

US FDA-registered facility supporting ANDA, NDA, and other US dossier submissions, with WHO Prequalification recognition for finished pharmaceutical products.

NAFDAC Nigeria Approved

Recognised by the National Agency for Food and Drug Administration and Control (Nigeria) for testing supporting Nigerian regulatory submissions.

Multi-Industry Analytical Scope

A single laboratory ecosystem covering pharma, nutraceuticals, cosmetics, food, medical devices, consumer products, packaging, and environmental products.

USD Pricing and SWIFT Invoicing

Quotes and invoices issued in USD or EUR on request. INR invoicing also available for India-registered entities. Proforma invoice issued before testing begins.

Chain-of-Custody DDP Sample Import

Established DDP sample import logistics, including import authorisation, NOC, end-use declaration, and customs brokerage coordination through DHL, FedEx, and UPS partners.

How It Works

Four steps from initial enquiry to a NABL-accredited international testing report.

01

Send Your Enquiry

Email or WhatsApp your regulatory target country and test scope. Your international account manager confirms the method, report format, and USD pricing within 24 hours.

02

Ship Your Sample

Ship under chain-of-custody documentation. Auriga handles import clearance through its established logistics protocol. Each sample is registered in YLIMS on receipt.

03

Testing and Review

Testing is completed against the confirmed method and results pass internal QA review before the report is generated.

04

Receive Your Report

Your NABL-accredited report is delivered digitally in your preferred format, accepted by your target regulatory authority. Raw data and audit trail are available on request.

Globally Recognised Accreditations

Accreditations and registrations referenced in our reports. Downloadable scope certificates are available on request for inclusion in regulatory submissions.

NABL Accredited

ISO/IEC 17025 accreditation recognised under the ILAC mutual recognition arrangement, accepted in 100+ countries.

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USFDA Registered

FDA Drug Establishment Registration for contract analytical testing. Reports referenced in ANDA, NDA, and 510(k) submissions.

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WHO PQ Listed

World Health Organization Prequalification listing supports WHO tender submissions and Global Fund procurement workflows.

GLP Certified

GLP-certified operations for nonclinical and analytical work where Good Laboratory Practice compliance is required by the receiving authority.

NAFDAC Nigeria

National Agency for Food and Drug Administration and Control (Nigeria) recognised for testing supporting Nigerian regulatory submissions.

APEDA and EIC

APEDA-approved since 2004 and EIC-recognised since 2007 for India-origin agri-commodity and food product exports.

Sample Import and Customs Guidance

Shipping analytical samples to India requires proper customs documentation. Our team guides you through every step to prevent delays at port.

Documentation We Provide

  • Import authorisation letter on Auriga Research letterhead
  • NOC (No Objection Certificate) for customs clearance
  • End-use declaration confirming samples are for testing purposes only
  • IEC (Importer Exporter Code) details for customs filing

Your Shipping Checklist

  • Commercial invoice marked "Samples for Testing, No Commercial Value"
  • Material Safety Data Sheet (MSDS) for chemical or pharmaceutical samples
  • Packing list with sample names, quantities, and batch numbers
  • Ship via DHL, FedEx, or UPS for reliable customs brokerage
  • Declare accurate HS codes; our team can provide the correct codes

Typical customs clearance time: 3 to 5 business days for standard analytical samples. Controlled substances and biological materials may require additional permits. Contact our team before shipping.

For detailed packaging and labelling instructions, see our sample submission guide.

Pricing and Payment

Transparent pricing in USD, EUR, or INR, with clear payment terms aligned to international buyer expectations.

Currency and Invoicing

  • Quotes issued in USD or EUR on request
  • INR invoicing also available for India-registered entities
  • Proforma invoice issued before testing begins
  • Final invoice with detailed test breakdown on completion

Payment Methods

  • Wire transfer (SWIFT), preferred for international clients
  • Bank details provided on proforma invoice
  • Payment due before testing begins (standard terms)
  • NET 30 credit terms available for repeat clients with approved credit

International pricing includes all standard testing, report generation, and digital delivery. Customs duties and shipping costs are borne by the client.

Countries We Serve

A representative sample of the 30+ countries where we have active client relationships. If your country is not listed, contact us. We have experience shipping samples from across the Americas, Europe, Africa, the Middle East, and Asia-Pacific.

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Request an International Testing Proposal

Reports accepted in 30 plus countries across pharma, nutraceuticals, cosmetics, food, medical devices, and consumer products. USFDA registered. WHO PQ. NAFDAC Nigeria approved. USD pricing and chain-of-custody sample import.

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