Veeva’s industry experience and technology solutions are empowering tobacco companies to transform their purpose and put health protection and harm reduction at the forefront.
The tobacco industry is part of a larger shift of consumer preferences away from traditional product formats to more innovative, sustainable formats. We see this in the shift from combustion-based vehicles to electric, from poultry towards plant-based alternatives, and similarly from traditional tobacco products to health protection and reduced-risk product offerings.
Transforming the business while facing new regulatory challenges is critical for the tobacco industry. Industry leaders are moving quickly to less harmful alternatives to reduce the burden of smoking-related diseases.
Veeva is helping tobacco industry leaders to navigate this transformation and while remaining compliant with stringent and evolving regulations. Veeva applies direct industry experience with relevant best practices from other highly regulated industries like life sciences, consumer products, and chemicals. This makes us uniquely suited to partner with tobacco companies as they drive innovation and diversify their offerings for a new vibrant era of next generation products (NGPs).
Leverage the best-in-class Life Science experience in managing Clinical Studies to substantiate product safety and overall harm reduction.
Ensure teams are developing reliable regulatory content to respond faster to changing regulations and authorities requirements.Speed-up EUTPD submission or PMTA approval by a defined list of requirements and expected documents depending on the NGP category and region.
Veeva already helps hundreds of life science customers manage their clinical trials and Streamline collaboration with third-party laboratories on toxicological and clinical testing based on your product type and reduce costs by reusing studies for similar E-liquids and devices.
Streamline the product journey and new product development using tools and processes to help you from start to finish.
Supporting manufacturing sites to achieve the 2030 targets set for waste. Innovating waste solutions for product disposal. Monitoring and responding to EU legislative changes, including the Single Use Plastics Directive.
Increased complaints and adverse events demands modern GxP quality platform.
Consumer Product & Chemical companies around the world are using Veeva to bring
high-quality and compliant products to market faster
Faster locating compliance related data & documents.
Of compliance process steps automated or eliminated.
Faster response time to regulatory information requests.
Improvement in data quality.
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.
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:
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.