400 Fountain Lakes Boulevard
St. Charles, MO 63301
Ph: 636.947.1200
Fax: 636.723.5888 |
Cetero’s St. Louis facility offers more than 20 years of clinical pharmacology experience to the pharmaceutical, biotechnology and generic industries. Designed to conduct studies in healthy participants and select special populations, St. Louis has completed more than 2,400 studies.
The purpose-built 520-bed facility was designed and operates with subject safety in mind. St. Louis’ experienced clinical staff consists of head medical director and principal investigator, Dr. Ramon Vargas, principal investigators, pharmacists, registered nurses, paramedics/EMTs certified clinical research coordinators and project managers all working together to ensure your study is completed right the first time.
St. Louis offers a wide range of Phase I study experience and a solid foundation of BA/BE expertise.
St. Louis’ database consists of more than 59,500 active healthy participants, special populations of smokers, non-smokers, postmenopausal women and elderly with access to three million people in the metropolitan area.
Our comprehensive Phase I capabilities, including protocol writing, project management, data management, PK/PD and biostatistics, bioanalytical, monitoring and medical writing, allow us to provide you with a full-service program of clinical drug development.
Contact us today to discuss your next project at 877.7CETERO or stlouis@cetero.com.
St. Louis Study Experience
- Absolute bioavailability
- Bioequivalence
- Interaction Studies
- Pharmacokinetic (PK)
- Dose proportionality and age/gender
- Pharmacodynamic (PD)
- Objective or subjective measures performed in-house or with patient diaries
- Medical Devices
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Cetero's Scientific Affairs Expertise
- Protocol Development
- Consultation
- Regulatory Affairs
- Data Management
- PK/PD
- Biostatistics
- Modeling and Simulations
- Medical Writing and ICH Reports
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St. Louis Facility
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