Clinical Trials

With MVG Consulting providing the all-important final piece, your clinical research project can achieve its objectives.

Our medical writers offer scientific communications, education material and medical writing consultancy, seamlessly becoming an extension of our clients’ teams. They accomplish this in multiple ways–by being flexible to the scope of the project, by using our expertise to guide through the clinical data and by demonstrating the efficacy of the drug and by improving […]

MVG is embarking on our industry specific newsletter & creating some free helpful resources for Clinical Research Teams.  If you have worked with us before, then you know that we are dedicated to providing senior level expertise on senior level projects. Specifically consulting with teams on:  Clinical Quality Assurance Clinical Monitoring SOP / Medical Writing  […]

The connection between MVG Consulting 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.

Our specialty is helping pharmaceutical and biotech companies with their clinical development programs by providing the necessary resources to begin clinical development programs.

Responsibilities included, but aren’t limited to: team coordination and training, investigator and subject recruitment, communications with sites and sponsor, project tracking and on-time reporting as well as meeting project timelines.

We provide companies alternatives to the large contract research organizations, helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.

–Full Standard Operating Procedures (SOPs) –Study & site startup activities –Documents and Submissions –IRB/EC meeting activity –Contracts & budgets –Screening and enrollment –Study subject activity throughout the trial –Regulatory documents (electronic and hard-copy) –Monitoring Visit Reports, calendars and schedules –Safety Reporting

Our knowledgeable and multilingual CQA (clinical quality assurance) auditors are well versed in local, national and international regulations, standards and guidelines.