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...
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.

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.

by | Nov 16, 2018 | Clinical Trials, Company News

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.

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