MVG Insights
Providing clinical development insight to the biotechnology and pharmaceutical industries
Featured News:
Moving into the Clinic…
Young biopharmaceutical companies go through a logical progression headed to clinical trials of the compounds that they have nurtured through discovery and research. Quality Systems in companies in their infancy are generally based on the principals of Good Laboratory...
TMF Management – How Important is it?
I always like to share topics that come up in audits that we are performing lately at MVG. A finding that keeps coming up repeatedly in several CRO vendor audits we have conducted is management of the Trial Master File by the CRO. Back in the days of a paper TMF, this...
A Leap of Faith in ’98
20 years ago this month I took a huge leap of faith and founded MVG Consulting Services. From a modest beginning, I have watched this company grow steadily over the years as MVG Consulting continues to expand our proficiency and expertise in an effort to deliver our...
MVG News:
Coronavirus Vaccine Clinical Trial Starting Without Usual Animal Data
Interesting read on the vaccine for COVID-19. While the speed at which Moderna has been able to progress their vaccine is impressive, it also raises many questions surrounding the bioethics of expediting such processes in the face of imminent need. Ethicists aren’t so...
MVG Consulting Services works closely with clients to ensure that all standard operating procedures are met.
This includes ensuring that your SOPs: –Are uniformly written with detailed instructions to record routine operations, processes and practices followed within a business organization –Contain adequate detail to clearly guide research staff through a particular...
MVG helps companies choose the best suited CRO alternative for their clinical study management needs.
MVG Consulting offers what some biopharmaceutical companies call a hybrid model approach to clinical study management that protects the sponsor from an under-performing full service CRO.
MVG Consultants are here to complete your puzzle, seamlessly integrating into your project team.
With MVG Consulting providing the all-important final piece, your clinical research project can achieve its objectives.
Inspection Readiness for Clinical Trials
MVG Consulting Service’s medical writing services include clinical and regulatory writing.
Our medical writers offer scientific communications, education material and medical writing consultancy, seamlessly becoming an extension of our clients’ teams. They accomplish this in multiple ways–by being flexible to the scope of the project, by using our expertise...
We Need Your Input!
MVG is embarking on our industry specific newsletter & creating some free helpful resources for Clinical Research Teams. If you have worked with us before, then you know that we are dedicated to providing senior level expertise on senior level projects....
MVG Consulting Services provides data management & biostats services to our clients.
The connection between MVG Consulting and our data management/biostatistics partners allow us to provide data management & biostats services to our clients, such as statistical programming, data collection, data management and data integration.
MVG Consulting Services gets clients through all clinical trial phases, from site prep to training.
Our specialty is helping pharmaceutical and biotech companies with their clinical development programs by providing the necessary resources to begin clinical development programs.
MVG Consulting’s clinical project managers are extremely customer-focused and directly accountable to the sponsor for all project-related responsibilities.
Responsibilities included, 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.
MVG Consulting takes pride in providing fully customized, high quality and cost-effective solutions.
We provide companies alternatives to the large contract research organizations, helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.
There are several advantages to partnering with MVG Consulting for Clinical Project Management.
–Full Standard Operating Procedures (SOPs) –Study & site startup activities –Documents and Submissions –IRB/EC meeting activity –Contracts & budgets –Screening and enrollment –Study subject activity throughout the trial –Regulatory documents (electronic and...