We believe that inspection readiness should be laid into the groundwork of all processes of clinical development. As such, we incorporate multiple strategies to achieve this, including:
–Standard Operating Procedures
–Monitoring procedures and activities
–Clinical site management
–Regulatory documentation review
–Vendor selection, management and oversight
–Investigator selection and management
–Trial Master File oversight
–Evaluation and reporting of adverse events and serious adverse events
–Training
–Investigational Medicinal Product (IMP) accountability and documentation
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.
