Clients

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Our Services

Phase I/IIa

We have an outstanding 35 years safe and compliant track record in Phase I/IIa drug development clinical trials.

 

Bioequivalence

We provide a wide range of services for bioequivalence and bioavailability studies to the generic industry.

 

505(b)(2)-Generic Hybrid

Through key alliances, our team of experts can help you design and conduct your 505(b)(2) study successfully.

 

Bioanalysis

Our bioanalytical facilities share more than 500 validated methods for drugs, metabolites and biomarkers. 

 

Central Lab

Our GLP/GCP compliant Central Laboratory Services provide essential supporting analyses for Phase I-IV trials.