UPCOMING EVENT

Regulatory submissions, information, and document management forum

Feb 14 - 16

DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum will feature industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related systems.

More infoWatch ReplayGet the ebookGet the case studyGet the data sheetGet the webinarGet the video
Regulatory submissions, information, and document management forum

Get the ebook

Get the case study

Get the webinar

Watch the replay!

Get the video

Get the data sheet

Thank you! Your resource is on its way to your inbox. If you do not receive an email in the next few minutes, please check your spam folder. Enjoy!
Thank you! We've sent you you details about accessing this event. If you do not receive an email in the next few minutes, please check your spam folder. Enjoy!
In the meantime, review this helpful content
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
A primer on medical device classification
A primer on medical device classification
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
Here's your video, enjoy!
Check out these additional resources
5 ways a RIM system can accelerate time-to-market for MedTech companies
5 ways a RIM system can accelerate time-to-market for MedTech companies
A primer on medical device classification
A primer on medical device classification
Quick reference guide - global medical device UDI requirements and timelines
Quick reference guide - global medical device UDI requirements and timelines
Oops! Something went wrong while submitting the form