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
