Leveraging Technology to Get Products to Market Faster...

Register to access another packed webinar as we explore our approach to speeding up time to market, through electronic submissions.


| This webinar is now available as a recording

Regulatory submissions are the most critical milestones in your clinical research program. Preparing and planning quality submissions can significantly accelerate time to market, maximize research investments and bring the benefit of new treatments to patience faster.

In our upcoming webinar, we will be exploring how technology can be leveraged to improve submission readiness and the quality of your electronic submissions. We'll start by diving in to why planning submissions is important, and explore some of the key components of a successful submission readiness plan.

We will also dive deeper into some of the tools Montrium has developed that give regulatory teams greater visitbility into the health and readiness of their submission, ultimately speeding up time to market.

The webinar will cover the following topics:

  • What are the regulations?
  • What are the regulatory challenges and how is regulation evolving?
  • Where is the industry today with electronic submissions
  • Why is submission planning important?
  • How can we create value with electronic submission software?
  • Submission Readiness strategy and important points to consider
  • Introduction to Montrium's Regulatory Tools
  • Plus much more....

The Presenter:

Paul Fenton

Paul Fenton

President & CEO - Montrium

ECM Software Provider

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