Modernize regulatory affairs with agility & transparency to respond to intensified regulations and evolving consumers preferences.

The Tobacco industry is seeing a real shift towards next generation and innovative new product development. This brings with it new complexities and regulation.

Veeva's Regulatory solutions help our customers ensure ongoing regulatory compliance across categories, channels, and geographies. Empowering organizations to accelerate Regulatory Affairs processes and maximize global transparency.

• 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 insight

Veeva's Quality 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.

When you are looking for a compliant, validated system to support your compliance initiatives across multiple products and sites. Your objective is to gain one global single source of truth that is future-proof, transparent, easy-to-use, flexible and scalable. Veeva QualityOne provides all of this. It is a complete and easy-to-use solution for document and records management.

It can also easily be leveraged to address your specific functional company needs. We go beyond being a technology vendor but will partner with you to streamline your work, accelerate speed to market, and reduce risk.

Increase fidelity of clinical studies to ensure product safety and assert & defend product claims of next gen’ products.

A mix of time to market, product efficiency, and product safety make Tobacco a unique industry in terms of clinical trials management. The Tobacco industry must benefit from solutions that are fully adapted and that allow a rapid response to the market and to regulatory constraints - including the management of company sponsors, CROs, and other study partners.

The Veeva Clinical Suite delivers a unified, cloud based solution to manage complex clinical studies. With applications focused on managing study documents (eTMF), data and processes (CTMS). The Veeva Clinical Suite allows Tobacco companies to coordinate global clinical trials, providing:

• 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

Veeva Claims is designed for marketing, legal and regulatory professionals to manage the end-to-end process for product and marketing claims. With core Claims Management, as well as capabilities for localization of global claims, challenge response, and oversight and insights into the global claims process, Veeva Claims helps companies reduce risk, accelerate time to market, and protect their brand.

• Veeva Claims integrates development, approval, usage and support into one truth that gives you confidence in claim management, use and response.
• Full detail on permissible usage by product, geography, and marketing channel
• Workflows for creation, substantiation, review and approval, with audit trails
• One click traceability from claim to substantiation and marketing assets using the claim
• Claim risk ratings with automated prompts and triggers for review workflows