MVG Insights
Providing clinical development insight to the biotechnology and pharmaceutical industries
Featured News:
No Results Found
The page you requested could not be found. Try refining your search, or use the navigation above to locate the post.
MVG News:
MVG Consulting’s clinical quality assurance services help our clients ensure the integrity of their clinical trials.
Our knowledgeable and multilingual CQA (clinical quality assurance) auditors are well versed in local, national and international regulations, standards and guidelines.
MVG is Hiring – Clinical Trial Managers
Are you a Clinical Trial Manager, Clinical Project Manager, or Medical Writer looking for your next career move? Contact MVG today with job inquiries!
Proper clinical monitoring ensures the integrity of trial data and the protection of the rights and well-being of study participants.
Our clinical research associates work closely with your team on protocol and indication training, building strong site relationships and ensuring site compliance.
Ready to file a marketing application such as a New Drug Application, Biologics Licensing Application or Marketing Authorization Application?
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...
MVG can assist at any stage of clinical trial development.
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.
MVG’s “project rescue” boasts a solid track record, using a well-proven model, to bring projects back on track.
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...
Virtual companies contract MVG Consulting Services to work in all aspects of clinical development.
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...
The phases of a clinical trial can be notoriously complex, and success begins with a solid plan.
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.
Our clinical research consultants are dedicated to the highest levels of professional service and support.
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.
Keep control of your clinical development project, while obtaining the necessary, high quality clinical research consulting MVG has become famous for.
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 Consulting Services has provided a role in the development and approval of many vitally important compounds in our 20 years.
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.
MVG Consulting Services provides the resources you need for your clinical development program.
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.