• Your Bridge to Better Medicines

  • Positive innovation

  • Attention to detail

We aim to become a valued partner for your product research, development and registration.

WHO WE ARE

Anapharm Bioanalytics is a GLP-certified, FDA-inspected, GCP-compliant and ANVISA-certified bioanalytical contract research organization (CRO) offering comprehensive high quality bioanalytical services to the pharmaceutical, biotechnological and generic industry worldwide.

PHASE I-III & BIOEQUIVALENCE

We provide full service outsourcing solutions to conduct preclinical, Phase I-III clinical trials and bioequivalence studies for registration worldwide. As a leading provider of bioanalytical services we aim to become a valued partner for your product research, development and registration.

INDUSTRY LEADER

We offer 30+ years of experience in analytical method development, validation and sample analysis of both small and large molecules in a variety of biological matrices using state-of-the-art LC-MS/MS and Ligand Binding Assay (LBA) technology platforms.

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bioanalytical methods

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studies performed

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samples per year

SERVICES

Method development, validation and quantitative sample analysis of small molecules and biologics at any stage of drug development from early preclinical across all phases of clinical development and bioequivalence.

Method list

Anapharm Bioanalytics offers an extensive list of validated analytical methods to support bioequivalence, drug-drug interaction and other types of studies. If you are unable to find the assay you need or require the development of a proprietary method, please contact us; we shall be glad to assist you.

Find your method here: