During this introductory and refresher training you’ll discover how you can reduce your workload by using Cortellis to track the ever-changing regulatory landscape for medical devices and IVDs. See how every member of your team, across all regulatory functions and responsibilities, can stay up-to-date and access the timely and accurate information needed to remain compliant, increase approval rates and enter new markets.
Join us to learn how to:
- Quickly identify up-to-date as well as historical guidelines and regulations for up to 74 countries and regions from the world’s largest network of regulatory documents.
- Create data-driven strategies for your regulatory functions across your countries and regions of responsibility by comparing key information at a glance – for example, labeling requirements, adverse incident reporting, marketing application procedures, post-marketing modifications, and more.
- Access exclusive English translations of local language documents plus other English language tools to help you market your devices and IVDs faster.
- Save time tracking changes – set up email notifications and allow Cortellis to tell you when there’s a new or updated document that could affect your company’s compliance.
The presenter will also be available to answer your questions. Join us online to learn more about Cortellis Regulatory Intelligence in 30 minutes + optional Q&A.