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COVID-19 has left a trail of uncertainty in its wake as the burden weighing on pharmaceutical companies working to get their clinical trials back on track appears somewhat insurmountable. These challenges facing the pharmaceutical industry are multifaceted as the number of trials previously put on hold now looking to reconvene is compounded by the growing […]

While the speedy development of a COVID-19 vaccine lends itself to a faster “return to normal”, the expedience raises some very legitimate concerns about the quality of such a rushed product. Due to the immense pressure to approve a vaccine quickly, a subpar and potentially dangerous vaccine may be on the fast track to approval […]

A look into Risk Evaluation and Mitigation Strategies (REMS) programs and how MVG can help. MVG Insights: REMS Monday, April 6, 2020 Risk Evaluation and Mitigation Strategies (REMS) programs were instituted as part of the FDA Amendments Act (FDAAA) in 2007 to provide safe access to products that may not otherwise be approved based on their […]

MVG is ready and able to assist in remote audits amongst travel restrictions caused by COVID-19.    Amidst the evolving challenges resulting from the COVID-19 outbreak, MVG can offer remote solutions to ensure maintained efficiency. Remote offerings, to help keep your timeline intact: Trail Master File Audits Clinical Study Reports (CSR) Audits Internal Audits Vendor […]

We offer clinical research consulting services, clinical trial development, and clinical research inspections preparedness. Contact MVG Consulting Services today to find out how our team can help your organization achieve its objectives.

MVG is experienced to help at every stage of the Clinical Trial Development process, so that sites and vendors are prepared for regulatory agency inspections. We can assist with Clinical Trial Development by helping sponsors before the study starts (Pre-Study), during an ongoing study to keep it on track (Ongoing Studies) or through other Marketing […]

Our medical writing services also offer scientific communications, education material and medical writing consultancy.

This includes ensuring that your SOPs: Are uniformly written with detailed instructions to record routine operations, processes and practices followed within a business organization Contain adequate detail to clearly guide research staff through a particular procedure Are aimed at a specific procedure but be written in a general format that can be easily followed so […]

The connection between MVG and our data management/biostatistics partners allow us to provide data management & biostats services to our clients, such as statistical programming, data collection, data management and data integration.