Upcoming training
Optimize your post-approval changes with Cortellis (30 mins plus Q&A)
Congratulations on your successful product approvals and launches. However, in order to gain and maintain a leading position, what is the best way to manage the post-approval processes and deal with changes, variations and supplements?
With Cortellis Regulatory Intelligence you have access to Regulatory Summaries, which summarize the key regulatory requirements for changes and provide a full variations submission procedures picture. For the specifics you can easily link out to the relevant local documents, such as guidelines. Written in English, the Regulatory Summaries are continuously maintained by content experts.
Join this webinar to learn how to facilitate your post-approval processes with Cortellis, covering as examples:
- Variation procedures and timelines
- Changes of manufacturing sites and processes
- Changes to packaging materials
This session will focus on lifecycle management and CMC-related changes in Cortellis Regulatory Intelligence.
Tuesday, February 26, 2019
9am New York/ 2pm London/ 3pm Paris
Register |
Wednesday, February 27, 2019
9am San Francisco/ 12pm New York/ 5pm London/ 6pm Paris
Register |
Thursday, February 28, 2019
9am London/ 10am Paris/ 2:30pm Mumbai/ 5pm Beijing
Register |