MVG Clinical Research Associates work closely with your team on building strong site relationships and ensuring site compliance. #MVG #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #biotechnology
At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of Investigator Recruitment, Site Selection, Regulatory Document Collection, Site Training, Clinical Monitoring (Qualifications, Initiation, Interim, and Close-out...
At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of Investigator Recruitment, Site Selection, Regulatory Document Collection, Site Training, Clinical Monitoring (Qualifications, Initiation, Interim, and Close-out...
At MVG, our highly-skilled clinical operations consultants have a high level of expertise in the areas of SOP Development, Protocol Development & Review, CRF Design, Informed Consent Form Development, Investigator Meeting Planning, and AE/SAE Reconciliation #MVG...
MVG’s clinical trial management services have helped numerous clients during all phases of project development. We pride ourselves in providing our clients with fully customized, high quality and cost effective solutions to meet all of their needs. #MVG...
At MVG Consulting, we attract senior level consultants who can provide our clients with the highest level of expertise in the areas of Project Management, Quality Assurance, Clinical Trial Management, Medical Writing and Clinical Monitoring. #MVG...
Clinical Monitoring is a quality control measure put in place to ensure that the integrity of trial data and protection of the rights and wellbeing of study participants are protected. MVG works closely with your team to set up a professional team of clinical research...
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.
