• Accelerate and unify regulatory requests, data and documents
• Enable global collaboration and coordination
• Simplify submission and registration management
• Unlock regulatory insights

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Quality and HSE Incident Management

Improve customer experience by maximizing product quality, ensuring compliance and accessing the digital quality customer voice.

• Transform feedback and KPIs into product and process insights and improvements
• Accelerate identification and resolution of complaints, non-conformances and incidents
• Unify Documents, Training, eQMS and HSE Incidents in a single, easy-to-use application
• Maximize supplier performance, response and compliance with digital supplier corrective actions, remote audits and automation of CoA inspections.

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Advertising Claims & Packaging Copy Management

Ensure global claims compliance by managing the end-to-end process for advertising claims and all elements on a package. 

• Full detail on permissible usage by product, geography, and marketing channel
• Workflows for creation, substantiation, review and approval, with audit trails
• Generate pack copy sheets automatically
• One click traceability from claim to substantiation and marketing assets using the claim
• Claim risk ratings with automated prompts and triggers for review workflows

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Study Management (Veeva Clinical)

The Veeva Clinical Suite delivers a unified, cloud based solution to manage complex studies. With applications focused on managing study documents, data and processes, as well as tracking payments to sites, company sponsors, CROs, and other study partners can now have full visibility into the process and a single source of truth for all study information.

• Provides real-time inspection readiness, full visibility into study completeness
• CRO’s gain the flexibility to efficiently populate studies
• Manage the entire end-to-end clinical study process and gain a global view into tasks in one unified system

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