Dedicated to the highest level of professional service and support in order to guide you through your clinical projects and help bring them to fruition. With our highly qualified clinical research professionals, you can be assured a seamless integration and successful outcome. MVG Consulting Services specializes in helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.
We can provide start-up and virtual companies with the necessary resources to begin their clinical development program. Established in 1998, MVG Consulting provides companies alternatives to the large Contract Research Organizations. Services provided by MVG include Clinical Research Consulting Services, Clinical Trial Development, Project Rescue, Inspection Readiness, CRO Alternative guidance.
We can provide start-up and virtual companies with the necessary resources to begin their clinical development program. Established in 1998, MVG Consulting provides companies alternatives to the large Contract Research Organizations. Services provided by MVG include Clinical Research Consulting Services, Clinical Trial Development, Project Rescue, Inspection Readiness, CRO Alternative guidance.
Services
Maryanne Visconti Gottfried is the President and founder of MVG Consulting Services. Inc. She started the company in 1998 to provide clinical research consulting services to smaller biotech and pharmaceutical companies as an alternative to using large CROs.
Maryanne is a clinical research professional with over two decades of experience in the biotechnology/pharmaceutical industry working at small to medium sized companies in several capacities including data management, medical writing, and clinical operations.She holds a Bachelor of Science Degree in Biology from Boston State College and a Master of Science in Business from Lesley University.
Maryanne is a clinical research professional with over two decades of experience in the biotechnology/pharmaceutical industry working at small to medium sized companies in several capacities including data management, medical writing, and clinical operations.She holds a Bachelor of Science Degree in Biology from Boston State College and a Master of Science in Business from Lesley University.
We pride ourselves in providing our clients with fully customized, high quality and cost effective solutions to meet all of their needs. Our drug development and clinical trial management services have helped numerous clients during all phases of project development.
A client working on a rare disease indication called MVG Consulting to help them get ready for a series of regulatory agency inspections at both their vendors and at their clinical sites due to a pending marketing application to be filed.The client had a history of poor performance and possible GCP issues internally and at their vendors and sites.
A client working on a rare disease indication called MVG Consulting to help them get ready for a series of regulatory agency inspections at both their vendors and at their clinical sites due to a pending marketing application to be filed.The client had a history of poor performance and possible GCP issues internally and at their vendors and sites.
The Clinical Operations function is a critical component in all studies. From start-up to close-out, our highly-skilled clinical operations consultants ensure proper planning, study conduct, patient safety and data quality, while fostering good communication between study sites and sponsors. MVG Consulting Clinical Trial Managers provide leadership and operational expertise through collaborative planning, implementation and execution.
Clinical Monitoring is a quality control measure put in place to ensure the integrity of trial data and protection of the rights and wellbeing of study participants are protected. An MVG Consulting Clinical Research Associate can function as a member of the study team and acts as a link between the study team and the sponsor.
MVG Project Managers are extremely customer-focused and directly accountable to the Sponsor for all project-related responsibilities which, among others, include team coordination and training, investigator and subject recruitment, communications with sites and sponsor, project tracking and on-time reporting as well as meeting project timelines.
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