Clinical Trials

MVG provides highly qualified clinical research professionals who become a part of your project team, seamlessly. Additionally, we provide virtual companies with an entire project team that encompasses all aspects of clinical development.

Let MVG Consulting conduct an analysis of your existing program. Keeping inspection readiness in mind through the entire program will help increase the odds of a successful inspection.

Many biopharmaceutical companies are choosing to take a hybrid approach to clinical study management, using multiple vendors to handle individual stages or parts of the project. This allows the sponsor to select their own vendors, rather than being forced into a CRO’s infrastructure. It has the added benefit of protecting the sponsor if a full […]

MVG Consulting has helped biotech and pharmaceutical clients succeed in all phases of project development and clinical research for over twenty years. MVG Consulting can help you choose the best suited CRO alternative for your clinical study management needs.

We believe that inspection readiness should be laid into the groundwork of all processes of clinical development. As such, we incorporate multiple strategies to achieve this, including: –Standard Operating Procedures –Monitoring procedures and activities –Clinical site management –Regulatory documentation review –Vendor selection, management and oversight –Investigator selection and management –Trial Master File oversight –Evaluation and […]

Our experience has been that many clients think about inspection readiness when an inspection is imminent due to the filing of a marketing application. However, we believe that inspection readiness should be part of the project at all phases. When we start a project with one of our clients, we help them incorporate strategies for […]

MVG Consulting Clinical Quality Assurance (CQA) services help our clients ensure the integrity of their clinical trials. The CQA audits we conduct include: clinical investigator site audits, working with sites to prepare for regulatory agency inspection, conducting GAP analysis to assess systems and procedures, as well as clinical study document reviews, database audits, vendor audits […]

Sometimes, things just don’t work out. When you reach an impasse with your CRO, when proper planning isn’t done, when the “A” team you were promised at the kick off meeting becomes the “B” or the “C” team, you need to rescue what you can, and return your project to its proper course. Drug development […]

If you have limited resources internally and need the services of a full service CRO, MVG Consulting can help manage the CRO for you via “Managed CRO Services.” We provide high level consultants who seamlessly integrate with your internal team, providing you with the resources you need to manage your CRO.

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 become a part of your project team.