At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of SOP Development, Protocol Development & Review, CRF Design, Informed Consent Form Development, Investigator Meeting Planning, and AE/SAE Reconciliation.

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.