MVG Consulting can help you with this process and get sites and vendors ready for regulator agency inspections, including: –Preparation of Common Technical Document sections –Preclinical –CMC –Clinical –Assessment of inspection readiness for sites and vendors –Inspection Readiness Training –Mock inspections at sponsor, sites and vendors –Planning post-marketing commitment studies
We help at any and all phases–before the study starts, during the study, and even through other marketing application services required after conducting a successful study.
When your best-laid plans can go awry, MVG Consulting Services can help. Our experienced consultants can address the most challenging situations. The old adage is true; we don’t live in a perfect world, and even the most carefully planned project can hit a bump in the road. MVG Consulting Services steps in seamlessly when a […]
In today’s digitally connected world, many successful companies have personnel scattered across the country, and MVG has provided, and continues to provide, entire project teams to start-ups and virtual companies in need of highly qualified clinical research professionals.
Good planning is especially important in all processes during the clinical development of your product. For 20 years, MVG Consultants has provided critical organization and support in vendor oversight and management, site prep, IMP management and training.
MVG Consulting Services’s highly-skilled clinical operations consultants ensure proper planning, study conduct, patient safety and data quality from start to finish, while fostering good communication between study sites and sponsors.
MVG Consulting has provided top-of-the-line clinical research expertise that has led to numerous successful projects, for 20+ years. Whether you need an entire project team, or just a bit of critical scaffolding to make your project stand, MVG can help.
MVG attracts senior level consultants who provide the highest level of expertise in the areas of Project Management, Quality Assurance, Clinical Trial Management, Medical Writing and Clinical Monitoring.
Our highly qualified clinical research professionals seamlessly become part of your team. Services provided by MVG include Clinical Research Consulting Services, Clinical Trial Development, Project Rescue, Inspection Readiness, CRO Alternative guidance.
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.