Globalization, supply chain complexity, patient safety, and new regulations are significantly impacting the total product lifecycle. Managing global compliance can involve more than 100 different systems and spreadsheets, often resulting in manual, cumbersome processes and a slower time to market.
Veeva MedTech enables medical device and diagnostics manufacturers to unify systems with a single source of truth for registrations management, submissions, and publishing to ensure global regulatory compliance and speed to market.
The RIM Suite is a unified group of cloud software applications that provides end-to-end visibility, oversight, and control for all regulatory compliance documents, data, and Health Authority correspondence, throughout the total product development lifecycle.
Unified RIM application for end-to-end regulatory compliance management
Modernizing Regulatory Affairs: 2021 Regulatory Benchmark Report
GE Healthcare: Seven KPIs to Measure RIM
Alcon and Terumo share key areas where digitalization can support global compliance