At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of Investigator Recruitment, Site Selection, Regulatory Document Collection, Site Training, Clinical Monitoring (Qualifications, Initiation, Interim, and Close-out visits), and Drug/Device Accountability.
An MVG Consulting Clinical Research Associate can function as a member of the study team and acts as a link between the study team and the sponsor. Clinical Monitoring is a quality control measure put in place to ensure that the integrity of trial data and well-being of study participants are protected. MVG works closely […]
MVG Consulting’s Clinical Trial Managers provide leadership and operational expertise through collaborative planning, implementation and execution. MVG Consulting can assist with your Clinical Trial Development by helping sponsors before their study starts, during an ongoing study to help keep it on track, or through other marketing application services required after conducting a successful study.
We pride ourselves in providing our clients with fully customized, high quality and cost-effective solutions to meet all of their needs. Contact us to learn more about MVG Consulting and how our team can help your organization achieve your objectives.
MVG provides qualified clinical research professionals who seamlessly become a part of your project team, covering all aspects of clinical development and research.
Since 1998, MVG Consulting has been providing companies with alternatives to the large Contract Research Organizations. Services include Clinical Operations, Clinical Monitoring, Clinical Project Management, Clinical Quality Assurance, Data Management, Medical Writing and S.O.P. Development.
MVG provides clinical research professionals with expertise in your required therapeutic indications, including hematology. These highly qualified consultants 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. MVG Consultants provide expertise in the following therapeutic indications: Hematology Oncology Vaccines […]
We support ongoing studies in a myriad of ways, including: Site Initiation and Monitoring visits Vendor Management and oversight Protocol Amendments Tracking patient enrollment Clinical Trial Material forecasting In process audits of vendors Review of Monitoring Reports for CRO-managed studies Prepare audit plan for site and vendor audits Writing IND annual reports and DSURs Ongoing […]
Services provided include Clinical Research Consulting Services, Clinical Trial Development, Project Rescue, Inspection Readiness, CRO Alternative guidance…essentially, MVG can provide a team that covers all aspects of clinical development.
As an alternative to large CROs, MVG provides highly qualified clinical research professionals who seamlessly become a part of your project team.