eWizard Content Experience Platform logo

eWizard Content Experience Platform

AI-powered content creation and management for pharma and life sciences commercialization, with compliance automation and multi-channel publishing.

Solution by Viseven
Visit website

Overview

eWizard Content Experience Platform, developed by Viseven, is an end-to-end content enablement solution designed for pharmaceutical and life sciences organisations. It supports the full content lifecycle — from creation and collaboration through to localisation, approval, and publication — with the goal of helping teams go to market faster while maintaining brand consistency and regulatory compliance. The platform serves both large enterprises and SMEs across pharma, biotech, and broader healthcare sectors.

eWizard incorporates AI and data analytics capabilities and is built to integrate with existing digital environments. It is used by global and local marketing, content, and medical-legal-regulatory (MLR) teams to coordinate content operations across functions and geographies.

Core Platform Capabilities

  • Centralise and collaborate: Content creation is centralised on a single platform that aligns global and local teams around shared goals. Non-technical colleagues can create and edit content without specialist skills, supporting cross-functional teamwork.
  • Plan, organise, and localise: Marketing campaigns can be planned and communicated within the platform. Teams can assign tasks, set deadlines, and use integrated calendars and dashboards to coordinate across internal teams and external vendors. Content can be adapted and translated to support a consistent global-to-local approach.
  • Publish, tag, and export: Content can be published directly to target systems. Advanced metadata tagging tools support quick content retrieval, and multiple export options allow content to be converted and published in formats compatible with various target systems.
  • Customisable solutions: The platform can be tailored to specific business requirements.
  • Integration: eWizard connects with existing digital environments and third-party systems, including Salesforce.

Reported Business Outcomes

  • Reduction in operational content production costs of up to 50%.
  • Acceleration of time to market by up to 45%.
  • Acceleration of the MLR review and approval process by up to 30%, reducing turnaround times and supporting faster regulatory approvals.
  • Improved content quality through standardised processes.
  • Increased customer satisfaction through delivery of personalised content experiences.
  • Concept-to-field-ready asset production in under six hours, supported by eWizard templates.

AI and Automation Features

  • AI-powered auto-tagging for content management, with one documented client case reporting a 340% ROI and a 60% reduction in manual tagging effort.
  • AI-assisted content creation and analytics to support content experience delivery.

Documented Client Results

  • A leading pharma company achieved 340% ROI and a 60% reduction in manual tagging through AI-powered auto-tagging implementation.
  • A pharma client saw a 5% increase in brand advocacy and a 42% increase in portal registration after improvements to accessible medical content delivery.
  • A biotech organisation used a Salesforce-integrated tool built by Viseven to manage large volumes of data.
  • A compliance management system implementation improved healthcare interactions for a client in the sector.

eWizard is deployed as a platform that integrates with existing digital infrastructure, including CRM systems such as Salesforce. It is positioned for use in regulated industries where MLR compliance, content traceability, and localisation at scale are operational requirements. Viseven provides ongoing support and partnership services alongside the platform.

Meta

Domain
Commercial & Medical Affairs
Subdomain
Medical Affairs Operations
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechMedical Devices
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
QA / Regulatory AffairsMedical Affairs ProfessionalCommercial / Market Access
Compliance standard(s)
GxP
Tag(s)
Uses AI