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At Aurigene Pharmaceutical Services we offer a wide range of integrated discovery biology services to meet your drug discovery needs. Our services include biochemistry and cell-based assays, DMPK, toxicology, microbiology and in vivo pharmacology.

Our team has the experience of successful regulatory filing with various global regulatory agencies. During the past two decades, our experienced and well-qualified team has been able to apply differentiated solutions to each aspect of discovery research, which has resulted in the discovery of many clinical candidates in collaboration with our clients. Numerous research publications and feedback from clients are a testimony of our success.

Our state-of-the-art toxicology facility in Hyderabad, India operates under GLP and has been audited by the US FDA and other regulatory agencies.

Why Aurigene Pharmaceutical Services?

World Class Labs

FDA audited and BSL-2 compliant microbiology lab, GLP accredited labs for bioanalysis, PK and toxicology studies.

Regulatory Submissions

+1000 efficacy studies and toxicity including submissions to US FDA and DCGI

Tailored Studies

Studies can be designed to comply with regulatory needs

Data Quality and Advisory

Highly reproducible data with interpretation advisory

Aurigene Pharmaceutical Services is

a leading CRO/CDMO

that provides contract research and manufacturing services

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