Founded in 1995, Cenetron is a central laboratory that operates worldwide, supporting clinical trials and pre-clinical drug development studies for pharmaceutical and biotechnology companies. Cenetron has remained true to its goal of providing high quality, cost effective testing services that enhance patient care. Located in Austin, Texas the company occupies a state of the art facility that serves as the central laboratory and home to its corporate offices.

Cenetron’s focus on clinical trials for antivirals, vaccines and therapeutic compounds has made us uniquely qualified to meet the demanding role that a laboratory partner must play during clinical development of these agents. Cenetron’s track record of innovation and scientific excellence in its laboratories has been critical to the company's successes. The heart of our R&D capabilities lie in the Technology Development Group (TDG). The TDG is capable of quickly designing, validating and implementing sponsor-defined assays. These assays can be offered in our central laboratory for testing during a clinical trial or transferred to the sponsor company through a tech transfer agreement.

In addition to our development services, Cenetron employs the latest in molecular technology platforms, including:

• TaqMan
• Molecular Beacons
• Real-Time PCR
• DNA Sequencing
• PCR
• NASBA
• LiPA

Applications of the above technologies have been useful in:

• Pharmacogenomics
• Allelic discrimination
• Viral load testing
• Viral genotyping
• Viral phenotyping
• Drug metabolizing enzyme genotyping (Cytochrome P450s)
• Drug Resistance testing

We also offer a variety of safety panel and routine tests:

• Hematology
• Serum Chemistries
• Serum Liver Enzymes
• Coagulation
• Urinalysis
• Viral Serology
• Biosafety Tests

• Provide physician review and consultation on the study protocol.
• Provide investigator site supplies that include custom collection kits, manuals and shipping materials.
• Assist in the design and implementation of studies that are customized to the drug and licensing requirements.
• Identify study sites and participate in investigator site visits.
• Manage specimen couriers and worldwide logistics.
• Project Manager as the point of contact for each study
• Reporting:
  • Enrollment and other reports provided to the sponsor as required.
  • Test results to sites - fax, regular mail, or encrypted email.
• Data management services that include custom database creation and data transfers to the specifications of the sponsor.
• Barcode-enabled specimen tracking system for archived samples and nucleic acids.
• Custom case report form development.

Having performed clinical trials during all phases of development, we have gained valuable knowledge and experience that benefits our clients. Whether it's a small phase I study or a large international phase III study, or perhaps it is a post-marketing phase IV, you can feel comfortable that Cenetron has the resources and reputation to make it a success. As an assurance, we welcome the opportunity to provide our potential clients with references.

Contact Information

Cenetron Diagnostics Clinical Trials
Dr. Dwight DuBois, Laboratory Director
2111 West Braker Lane, Suite 300 
Austin, TX 78758 USA
Phone: 888-834-6632 x102
Fax: 512-439-5000
E-mail:

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