Resources

 

Scientific Posters

Pharmacokinetics of Subcutaneously-administered CBX129801, A Long-acting Synthetic C-peptide, in Patients with Type 1 Diabetes Mellitus
AAPS National Biotechnology Conference - May 2013
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Comparison of Encapsulated and Non-encapsulated Doxorubicin Pharmacokinetics Following Single Intravenous Administration of ATI-0918, an Encapsulated Liposomal Formulation, and DOXIL® in Female Rats
AAPS National Biotechnology Conference - May 2013
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Brochures

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Contract Research Services
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Method Development & Validation
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Non-Proprietary Assay List
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Drug Metabolism (DMPK) Assays
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Protein Binding Assays
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Dose Formulation Analysis
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Bioanalytical Services
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Immunoassays & Bioassays
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Pharmacokinetic Analysis
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Specimen Collection Kits
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Specimen Collection Kit Supplies
 

Presentations

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Company Overview
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A Novel Approach to
Internal Standardization
in LC/MS/MS Analysis
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In vitro Assays to Support
IND Submissions
 
 

Case Studies

The development of a non-traditional internal standard by derivatization allowed our client to maintain their rigorous timeline without resorting to an expensive synthetic effort.
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Employing selective extraction in method development enabled the accurate determination of in vivo drug concentration in plasma samples collected during our client’s Phase I trial.
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Customizing specimen collection kits for specific clinical trial sampling requirements streamlined our client’s Phase I study and helped ensure that all specimens collected were stabilized, properly labeled, and provided accurate pharmacokinetic data.
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Increasing assay sensitivity to determine drug concentration in epithelial lining fluid (ELF) samples allowed our client’s clinical trial to proceed uninterrupted, saving them time and resources.
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