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.
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 […]
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, […]
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.
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.
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.
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.
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.
Each individual clinical trial phase is important and necessary to ensure the effectiveness and safety of new drugs, medications and treatments. In conducting each phase, you need qualified clinical research professionals who can seamlessly fit with your team and propel the project forward. MVG Consulting specializes in providing these resources, since 1998.
Since our beginnings 20 years ago, we have always been rooted in the belief that small to medium–sized biopharmaceutical companies are overlooked in the world of larger CROs, and that we could help sponsor companies by providing the necessary scaffolding, in the form of our consultants, to support clinical projects.