Newsroom

Vitrana adds another Milestone to its ongoing successful implementation of TransformPV with one of the largest pharmaceutical organisation “Live” with TransformPV for meeting FDA eMDR requirement. The organization has implemented Vitrana’s TransformPV solution to meet its R3 eMDR regulatory requirements. TransformPV has enabled them to:

• Avoid the double data entry in source system (Argus) and eSubmitter
• Submit and track eMDR report through source system (Argus)
• Have single source of truth for data entry and submission tracking
• Easy to understand R2-HL7 side by side, which takes away the difficulty of understanding HL7 structure for the business users