Auriga Research serves clients across 30+ countries with globally accredited analytical testing. Our NABL, USFDA, and WHO PQ credentials are accepted by regulatory agencies worldwide. We handle sample import logistics, provide USD/EUR invoicing, and deliver reports that meet international filing requirements.
Our laboratory accreditations are accepted by regulatory agencies in every major pharmaceutical and food market. Downloadable certificates are available for inclusion in your regulatory submissions.
ISO/IEC 17025 accreditation recognized under ILAC mutual recognition arrangement, accepted in 100+ countries.
View Details →FDA Drug Establishment Registration for contract testing. Reports accepted for ANDA, NDA, and 510(k) submissions.
View Details →World Health Organization Prequalification listed laboratory. Reports accepted for WHO tender submissions and Global Fund procurement.
Shipping analytical samples to India requires proper customs documentation. Our team guides you through every step to prevent delays at port.
Typical customs clearance time: 3-5 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.
International pricing includes all standard testing, report generation, and digital delivery. Customs duties and shipping costs are borne by the client.
We regularly work with clients in these markets. If your country is not listed, contact us — we have experience shipping samples from 30+ countries.
United States
Germany
Japan
Australia
United Kingdom
Brazil
Netherlands
Our international coordination team responds within 24 business hours. Share your requirements and we will provide a detailed quote with import guidance.
Download a practical testing guide tailored to your industry — checklists, parameters, and regulatory tips in one place.
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