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 #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #clinicaloperations
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 #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #clinicaltrialmanagement #projectdevelopment
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 #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech
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 associates to manage your study at clinical sites across the […]
MVG Consulting’s Clinical Trial Managers provide leadership and operational expertise through collaborative planning, implementation and execution. #MVG #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #clinicaltrials
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.
Young biopharmaceutical companies go through a logical progression headed to clinical trials of the compounds that they have nurtured through discovery and research. Quality Systems in companies in their infancy are generally based on the principals of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP). Companies with GLP/GMP-based Quality Systems often are challenged by […]
Our MVG Consulting Clinical Quality Assurance services help our clients ensure the integrity of their clinical trials and protect research subjects’ rights and welfare. #MVG #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #qualityassurance
Our Clinical Research Associates will provide your team protocol and indication training to ensure the integrity of your trial data while protecting the rights and wellbeing of study participants. #MVG #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #team #protocol #training
Our Clinical Research Associates will provide your team protocol and indication training to ensure the integrity of your trial data while protecting the rights and wellbeing of study participants. #MVG #MVGConsultingServices #ConsultingServices #Consulting #Pharma #BioTech #team #protocol #training