How Technology Simplifies Regulatory MedTech compliance

With European MDR coming into force in May 2021, and IVDR in 2022, medical device and diagnostics companies need to move fast to address new requirements and mitigate the potential impact on the product lifecycle and their bottom line.

As a result, many organizations are turning to technology to achieve compliance and long-term sustainability of regulatory operations.

Watch Veeva MedTech presentation from the MedTech Summit event, where we uncover the key attributes that you should be looking for in the software. The session also highlights:

• Managing regulatory information in a dynamic global environment
• Keeping up with the pace of international regulatory change
• Improving efficiency through a global platform approach
• Driving process consistency, addressing regulatory complexity, and speeding time to market

EU MDR and IVDR preparation was a key theme at Veeva Medical Device and Diagnostics Summit. Hear from Alcon, GE Healthcare, Baxter, Roche Diagnostics and more, as they share their views and best practices to achieve sustainable compliance. Watch customer sessions on-demand today.