From enterprise to small and medium-sized companies-Veeva MedTech cloud solutions remove complexity and data silos by creating a single, unified source of truth across documents, data, and processes. Every step of the product life cycle is streamlined and connected with our solutions platform so you can get products to patients faster.
Increasing demand for real-world evidence, data, and stringent global regulatory requirements makes clinical research more complex, resulting in longer product development cycles. The ability to streamline clinical study processes and data management is crucial to driving innovation and getting medical devices and diagnostics to market quickly.
Globalization, supply chain complexity, patient safety, and new regulations significantly impact the total product lifecycle. Managing global compliance can involve over 100 different systems and spreadsheets, often resulting in manual, cumbersome processes and a slower time to market.
Veeva MedTech helps provide regulatory information management capabilities on a single, cloud-based platform, which streamlines global processes, improves the data quality, and helps MedTech companies adapt faster to regulatory environment changes and respond to Health Authority requests at any time.
With an ever-increasing focus on patient safety, quality management requires deep insights and trend analysis to ensure rapid innovation.
Veeva MedTech Quality Suite connects global processes, content, and functions, enabling medical device, diagnostic and therapeutic companies to manage all quality aspects in one place effectively.
Connecting the right content to stakeholders across multiple channels and interactions is a challenge for sales, marketing, and medical affairs teams in today’s increasingly complex MedTech world.
Veeva’s Commercial Cloud unifies stakeholder data, commercial and medical content, and customer engagement activity in a single platform while maintaining the boundaries required for compliance.
Thousands of customers, from emerging companies to Fortune Global 500, trust Veeva to manage their most important processes, documents, and data to bring their products to patients faster.
Founded in 2007, Veeva has been committed to innovation, product excellence, and customer success. Veeva provides cloud software, data, services, and consulting, helping more than 1,200+ customers, ranging from the world’s largest pharmaceutical, medical device, and diagnostics companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America.
1,200+ customers worldwide
125+ countries
27 offices worldwide
27 languages supported
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