Bioanalytical Services

Simple to Complex — Bioanalytical Validation Methods

Bioanalytical expertise provides quantitative measurements on a range of active drugs, from small molecules to peptides as well as metabolites. We can perform analysis in simple buffer matrices or complex biological matrices such as plasma, serum, urine, feces, bile and tissue. All Bioanalytical projects, from the simplest sample preparation and analysis to the most complex method validation, are approached with a focus on accuracy, precision, efficiency, and speed.
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"4P Therapeutics has been very happy with the bioanalytical services provided by Absorption Systems. They perform great work with rapid turnaround times at a resonable price. Our success is dependent on partnering with a service provider who we can count on to perform quality work under tight deadlines."

~ Alan Smith, Vice President, Clinical, Regulatory and Operations
4P Therapeutics

Bioanalytical Services

We offer a full range of bioanalytical services supporting drug discovery to all stages of clinical phases to pinpoint the detection of your compound

Bioanalytical Capabilities

We offer GLP and non-GLP method development and sample analysis, with the rigor required to satisfy regulatory agencies. We routinely provide bioanalysis for ADME screening, preclinical pharmacokinetic (PK), toxicokinetic (TK) studies, metabolite identification, and GLP bioanalysis of plasma samples from human clinical trials. We can now offer radioactive drug detection. Our labs are equipped with 21 LC-MS/MS systems, allowing for analysis of thousands of samples a day. We can handle projects ranging in size from a few to several thousand of samples.

Bioanalytical Instrumentation

Thermo Scientific LTQ Orbitrap XL
AB Sciex 4000 QTRAP
AB Sciex API 4000
Waters Acquity UPLC
Leap CTC Analytics Autosamplers
Tomtec Quadra 96 robotic sample prep workstation
Conventional HPLC with UV detection
Fluorescence detectors
Scintillation counters

All Studies Supported

Clinical Bioanalysis
GLP Bioanalysis
Non-GLP Bioanalysis
Method Development
Metabolite Identification

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Electronic Reporting and Documentation

LC-MS/MS data is generated using Analyst® Version 1.4.1 compliant with 21 CFR Part 11, and all customer reports are archived in a validated NuGenesis 7.0 database compliant with 21 CFR Part 11.

Learn more about Clinical/GLP Bioanalysis
Learn more about Metabolite Identification

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