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Services Bioanalysis

The focus of Magellan Bioanalytical is to help you achieve your preclinical or clinical goals by providing quality data delivered on time. Our experienced scientists at Magellan Bioanalytical provide you with resources by functioning as an extension of your own facility. Your resources at Magellan include the following bioanalytical services to support toxicology, preclinical, and clinical studies:

  • Automated online LC/MS/MS
  • ELISA
  • Surrogate markers
  • Clinical pharmacogenomics
  • Method development
  • Method validation of NCEs or established compounds to full GLP requirements
  • High throughput sample analysis to the high standards of GLP

We have extensive experience with the following studies:

  • Toxicokinetics
  • Short and long term toxicology studies
  • Pre-clinical studies
  • Clinical – all phases of clinical trials including phase I-IV

Our scientists' extensive pharmaceutical experience allows us to provide you with unsurpassed quality through a synergistic approach to help you meet your goals. We utilize automated online extraction technology coupled with tandem mass spectrometry to provide reproducibility data, which allows our scientists to focus on the scientific management of your project. Our experience, open communication, and cutting-edge innovation combine to provide the highest quality scientific results.

EXPERIENCE
QUALITY
PARTNERSHIP
INNOVATION

Experience
  • Effective project design
  • Timely project execution
  • Appropriate data interpretation
Partnership
  • Extension of your own facility
  • Direct contact with project scientists
  • Timely and open communication
Innovation
  • High-throughput processes increase productivity
  • On-line Q.A.: minimizes Q.A. "bottleneck"
  • Automated systems allow rapid data generation and increased focus on management of projects

Please call us with any questions or submit a project to us online.

Bioanalytical Services

  • LC/MS/MS
  • ELISA
  • Surrogate Marker
  • Automated Online Sample Analysis
  • Method Development
  • Method Validation
  • Full GLP Compliance
  • Electronic Data Management

Discovery Support

  • In-vitro Screening For Metabolic Stability
  • Structural Determination
  • Rapid Method Development Using LC/MS/MS
  • In-vivo Pharmacokinetics

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