MVG Insights
Providing clinical development insight to the biotechnology and pharmaceutical industries
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MVG Consulting clinical quality assurance services help our clients ensure the integrity of their clinical trials.
Our knowledgeable and multilingual clinical quality assurance (CQA) auditors are well versed in local, national and international regulations, standards and guidelines.
There are many advantages to partnering with MVG Consulting for Clinical Project Management.
Development of SOPs (Standard Operating Procedures) Study & site startup activities Documents and Submissions IRB/IEC interaction Contracts & budgets Screening and enrollment Study subject activity throughout the trial Regulatory documents (electronic and...
Clinical Monitoring ensures the integrity of trial data and the protection of the rights and well-being of study participants.
MVG clinical research associates work closely with your team on protocol and indication training, building strong site relationships and ensuring site compliance.
MVG Consulting Services takes pride in providing fully customized, high quality and cost-effective solutions.
MVG provides companies alternatives to the large contract research organizations, helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.
Moving toward filing a marketing application such as a New Drug Application, Biologics Licensing Application or Marketing Authorization Application?
Let MVG Consulting help you with this process and get sites and vendors ready for regulator agency inspections. MVG can help with: Preparation of Common Technical Document sections Preclinical CMC Clinical Assessment of inspection readiness for sites and vendors...
When your best-laid plans can go awry, MVG Consulting Services can help.
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’s “project rescue” boasts a solid track record, using a well-proven model, to bring projects back on track. Our experienced consultants...
Virtual companies contract MVG Consulting to work in all aspects of clinical development.
In today’s connected world, many successful companies have personnel scattered across the country, and MVG has provided, and continues to provide, when needed, entire project teams to start-ups and virtual companies in need of highly qualified clinical research...
MVG clinical research consultants are dedicated to the highest levels of professional service and support.
Our 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.
When it comes to Clinical Trial Development, MVG Consulting can assist at any stage.
We help sponsors before the study starts, during the study, and even through other marketing application services required after conducting a successful study.
The planning of a clinical trial can be notoriously complex, and success starts with a solid plan.
Good planning is vital in all processes during the clinical development of your product. For 20 years, MVG Consulting has provided critical organization and support in vendor oversight and management, site prep, IMP management and training.
Maintain control of your clinical development project, while obtaining the necessary, high-quality clinical research consulting from your trusted team at MVG Consulting.
For 20 years, MVG Consulting has provided top-of-the-line clinical research expertise that has led to numerous successful projects. Whether you need an entire project team, or just a bit of critical scaffolding to make your project stand, MVG can help.
MVG clinical project managers are extremely customer-focused and directly accountable to the sponsor for all project-related responsibilities.
These responsibilities include, but aren’t limited to: team coordination and training, investigator and subject recruitment, communications with sites and sponsor, project tracking and on-time reporting as well as meeting project timelines.