We support ongoing studies in a myriad of ways, including:
- Site Initiation and Monitoring visits
- Vendor Management and oversight
- Protocol Amendments
- Tracking patient enrollment
- Clinical Trial Material forecasting
- In process audits of vendors
- Review of Monitoring Reports for CRO-managed studies
- Prepare audit plan for site and vendor audits
- Writing IND annual reports and DSURs
- Ongoing document collection from sites
- Maintenance of Trial Master File
- Clinical Study Report development
MVG Consulting Services specializes in helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs and we can provide start-up and virtual companies with the necessary resources to begin their clinical development program.
Services include:
- Clinical Research Consulting Services
- Clinical Trial Development
- Project Rescue
- Inspection Readiness
MVG provides highly qualified clinical research professionals who seamlessly become a part of your project team. Additionally, we provide virtual companies with an entire project team that encompasses all aspects of clinical development.
We invite you to fill out the form below to learn more about how MVG Consulting can help you with your clinical devleopment needs.
