Dec 10th at 11 AM – 11:30 AM PST | 2 PM – 2:30 PM EST

With the increasing complexity of the global regulatory landscape, Regulatory Information Management (RIM) is at the heart of the decision making process for pharmaceutical and medical device companies. But what exactly does this mean?

In this 30 minute webinar, Ennov’s regulatory experts will explain the following key RIM concepts:
• A single entry point for all regulatory activities
• Creation of the product database
• Data integrity and reliability
• Integration with existing systems
• XEVMPD and IDMP compliance

This is the first in a series of three RIM webinars. The second webinar will feature Ennov’s RIM solution and the third webinar will take a deeper dive into the subject of IDMP.