Clinical Trials

Clinical Trials, Clinical Research Management, Clinical Trial Research Consulting, CRO Consulting, Clinical Research Consulting

MVG provides entire project teams of highly qualified clinical research professionals to virtual companies in the biotech and pharma space.

August 7th, 2019 | Clinical Trials

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.

MVG Consulting Services provides clinical research professionals for biotech and pharmaceutical companies’ clinical development programs.

August 5th, 2019 | Clinical Trials

As an alternative to large CROs, MVG provides highly qualified clinical research professionals who seamlessly become a part of your project team.

Through our staff expertise, MVG Consulting offers clients the highest level of professional service and support.

July 30th, 2019 | Clinical Trials

As an alternative to the large CROs, MVG guides our clients through clinical projects, and help bring them to fruition. For over 20 years, we have helped small to mid-sized biopharmaceutical companies maintain control of their development and conduct successful research and trials.

Quality Systems in new companies are generally based on the principles of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).

July 26th, 2019 | Clinical Trials

Companies with GLP/GMP-based Quality Systems are often challenged by the possibility of clinical trials and how to adapt their systems to a Good Clinical Practice (GCP) environment. MVG Consulting Services can perform an assessment of what is needed to support clinical trials. Contact us for more information on how MVG can assist your company as […]

MVG Consulting Services is often asked to come into a company and assess what is needed to support clinical trials.

July 24th, 2019 | Clinical Trials

This can include a Gap Assessment of the current system to review where they stand and how it can be adapted to a GCP environment. A Gap Assessment will be conducted to look at the Standard Operating Procedures (SOPs) to determine which SOPs are necessary at their stage of development. When the assessment is complete, […]

From Hematology to Neurology to Pain Management, MVG Consulting can provide the experts you need when conducting clinical trials.

July 22nd, 2019 | Clinical Trials

A short list of the therapeutic indications that MVG Consultants can help with their expertise: Hematology, Oncology, Anti-infectives, Vaccines, Cardiovascular, Pain Management, Infectious Disease, Inflammation, Women’s Health, Neurology, Rare Diseases, and Endocrinology. Contact us to learn more about MVG Consulting and how our team can help your organization achieve your objectives.

MVG Consulting helps rescue mismanaged clinical research projects.

July 18th, 2019 | Clinical Trials

In an unfortunate situation of project mismanagement, MVG Consulting has been called, time and again, to help our clients address the issues and get the project back on track. Whether due to staff turnover, site issues, monitoring issues, or other issues, projects can go astray. MVG can help.

MVG Consulting provides an alternative to the large Contract Research Organizations.

July 16th, 2019 | Clinical Trials

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.

We’re here to complete the puzzle.

July 12th, 2019 | Clinical Trials

From site prep to training, MVG Consulting can help assemble the puzzle pieces, seamlessly becoming part of your project team during the complex phases of your clinical trial.

Inspection Readiness is of utmost importance.

July 10th, 2019 | Clinical Trials

When we start a project with one of our clients, we incorporate strategies for a successful inspection that can be followed throughout the development lifecycle of a product. We strongly believe that this “inspection readiness” should be built in to the project from the start, greatly increasing the odds of a successful inspection.