Each individual clinical trial phase is important and necessary to ensure the effectiveness and safety of new drugs, medications and treatments. In conducting each phase, you need qualified clinical research professionals who can seamlessly fit with your team and propel the project forward. MVG Consulting specializes in providing these resources, since 1998.
Since our beginnings 20 years ago, we have always been rooted in the belief that small to medium–sized biopharmaceutical companies are overlooked in the world of larger CROs, and that we could help sponsor companies by providing the necessary scaffolding, in the form of our consultants, to support clinical projects.
MVG is experienced to help at every stage of the Clinical Trial Development process, so that sites and vendors are prepared for regulatory agency inspections. We can assist with Clinical Trial Development by helping sponsors before the study starts (Pre-Study), during an ongoing study to keep it on track (Ongoing Studies) or through other Marketing […]
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 […]