- Clinical investigator site audits
- Work with high enrolling sites to prepare them for possible regulatory agency inspection
- Conduct GAP analysis for sponsors to assess their systems and procedures to ensure compliance with applicable regulations
- Clinical database audits and study report reviews
- Clinical study document reviews
- System audits, in which we assess a client’s standard operating procedures (SOPs), processes and staff training programs and recommend improvements where needed
- Vendor audits, in which auditors evaluate a client’s vendors to ensure they have sufficient capacity and capability to deliver quality products and services on time and in compliance with regulations
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.
