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 visits), and Drug/Device Accountability.

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 visits), and Drug/Device Accountability.

by | Dec 7, 2018 | Clinical Trials, Company News

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.

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.

by | Dec 4, 2018 | Clinical Trials, Company News

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...

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