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VST’s Global Clinical Development covers every aspect of clinical research, from individual Phase I studies to complete Phase IV programs as well as coordinating international multi-center trials. We work across many therapeutic areas and have experience with a wide range of product types, including vaccines, biologics, orphan drugs, and devices.

Recognizing that no two projects are the same, VST provides a flexible service that is customized to meet the requirements of the individual client and project. Our experienced staff can take full responsibility for a project, from protocol design, study coordination, data management and statistical analysis, right through to the submission of the final clinical study report. Or, we can provide a stand-alone service to give you the exact level of support you need to ensure a successful outcome.
We also recognize the need for you to retain control and ownership of your projects, which is why we establish a comprehensive communication plan at the start of each project to ensure that all parties are fully informed of the project status at all times.

Benefits

  • Full-service capabilities resulting in cost and process efficiencies
  • Broad geographic reach giving clients access to wider patient populations
  • Qualified, trained staff in ICH, GCP, SOPs, and specified therapeutic areas
  • Flexible service offerings to meet the individual needs of the client and project
  • Upfront strategic planning to ensure a clear, concise development plan
  • Collaborative partnership with clients based on open communications

Services

  • Project management
  • Monitoring and site management
  • Feasibility studies
  • Phase I-IV program management
  • Full service (protocol design to clinical study report)
  • Pharmacovigilance and medical monitoring
  • Safety reviews