MVG Insights
Providing clinical development insight to the biotechnology and pharmaceutical industries
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MVG News:
If your clinical research studies have been mismanaged by a CRO, consider bringing MVG Consulting for a “project rescue.”
We have all worked in companies where perhaps planning wasn’t properly done, a CRO or other vendor was not vetted appropriately, or the “A” team you were promised at the kick off meeting with the CRO becomes the “B” or the “C” team. MVG Consulting can help to rescue...
MVG Consulting Services provides qualified clinical research professionals who seamlessly integrate with your project team.
Contact us to learn more about how our team can help your organization achieve your clinical research objectives.
MVG Consulting provides an alternative to the large Contract Research Organizations.
We can help you choose the best suited CRO alternative for your clinical study management needs. MVG offers a Hybrid Model approach to clinical study management which protects the sponsor from an under-performing full service CRO.
MVG Consulting gets our clients through all clinical trial phases, from site prep to training.
Our specialty is helping biotechnology and pharmaceutical companies with their clinical development programs by providing the necessary resources to begin clinical development programs.
MVG Consulting’s medical writing services include clinical and regulatory writing.
Our medical writing services also offer scientific communications, education material and medical writing consultancy.
The team at MVG Consulting Services works closely with our clients to ensure that standard operating procedures are developed that are user-friendly for the stage of development of the sponsor.
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 procedure...
MVG Consulting provides data management & biostats services to our clients.
The connection between MVG 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 Consultants complete your puzzle, seamlessly integrating into your project team.
With MVG Consulting providing that all-important last piece, your clinical research project can achieve its objectives.
MVG Consulting helps companies choose the best suited CRO alternative for their clinical study management needs.
MVG 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 Consulting’s medical writers become 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 to guide through the clinical data and by demonstrating the efficacy of the drug and by improving patient safety.
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...