April, 2019 | MVG Consulting Services

Good planning at the beginning of the program can lessen, or even prevent, many of the issues found during an inspection.

by MVG Consulting | Apr 30, 2019 | Clinical Trials

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.

MVG Consulting provides contract staff to help manage vendors in use during a clinical study.

by MVG Consulting | Apr 25, 2019 | Clinical Trials

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...

Fully customized, high quality and cost-effective drug development and clinical trial management services.

by MVG Consulting | Apr 23, 2019 | Clinical Trials

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.

During clinical development of a product, MVG helps incorporate strategies for a successful inspection.

by MVG Consulting | Apr 18, 2019 | Clinical Trials

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...

Keeping an Inspection Readiness mindset throughout your clinical development program increases the odds of a successful inspection.

by MVG Consulting | Apr 16, 2019 | Clinical Trials

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...

Good clinical practice requires high standards

by MVG Consulting | Apr 12, 2019 | Clinical Trials

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...

What do you do when your studies have been mismanaged by a CRO?

by MVG Consulting | Apr 8, 2019 | Clinical Trials

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...

Managing your Contract Research Organization

by MVG Consulting | Apr 4, 2019 | Clinical Trials

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...