Consumer Goods Solutions

• Simplify product compliance with one global, transparent view of regulatory knowledge
• Single source of truth for global registrations, while accounting for local market variation
• Accelerate and unify regulatory requests, data and documents
• Enable global collaboration and coordination
• Third party and retailer certification management
• Use analysis capabilities to unlock new regulatory operations insights

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QHSE Management

Veeva's Quality, Health, Safety and Environment (QHSE) capabilities cover product and process compliance to ensure safe, high quality products, as well as health and safety to keep workers safe and factories compliant. 

• 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 while accelerating time to market by managing the end-to-end lifecycle for advertising claims and all other elements on packaging. 

• Full detail on permissible usage by brand, product, geography, and marketing channel
• Workflows for claim creation, substantiation, review and approval, with audit trails
• Generate packaging briefs automatically from a system of record
• One click traceability from claim to substantiation and marketing assets using the claim
• Claim risk ratings with automated prompts and triggers for review workflows and expiration dates

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Veeva Clinical Suite

The Veeva Clinical Suite delivers a unified, cloud based solution to manage complex clinical 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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