MVG has been providing Clinical Operations, Clinical Monitoring, Clinical Project Management, Clinical Quality Assurance, Data Management, Medical Writing and S.O.P. Development solutions since 1998. Our highly qualified clinical research professionals seamlessly...
Good planning at the beginning of the program can lessen, or even prevent, many of the issues found during an inspection. Let MVG Consulting conduct an analysis of your existing program. Keeping inspection readiness in mind through the entire program will help...
Clinical investigator site audits Work with high enrolling sites to prepare them for possible regulatory agency inspection Conduct GAP analysis for sponsors to assess their systems and procedures to ensure compliance with applicable regulations Clinical database...
From start to finish, our highly-skilled clinical operations consultants ensure proper planning, study conduct, patient safety and data quality. MVG Consulting Clinical Trial Managers provide leadership and operational expertise through collaborative planning,...
In this model, you choose which services to outsource to a CRO and which services you will manage through vendors of your choosing. MVG Consulting can provide contract staff to help manage the various vendors in use during a study. We can also help in the search for...
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...
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.
Our specialty is helping biotechnology and pharmaceutical companies with their clinical development programs by providing the necessary resources to begin clinical development programs.