Event / Webinar

How technology optimizes the publishing process for regulatory submissions

Regulatory submissions are one of the most critical milestones for Life Sciences organizations and can consist of thousands of documents. Submitting on time and in full compliance with Regulatory Agencies' requirements remains a challenge for many companies.

On-Demand 1 hour Your Desk!

REGISTER NOW

**For more information, please see Cencora PharmaLex Privacy Policy. If you do not wish to receive any communication from us, you may unsubscribe at any time.

Speakers

Jennie May

Director, Regulatory Informatics and Operations, PharmaLex

Paul Ireland

VP Life Sciences, DocShifter, Belgium

Life Sciences organizations adopt cutting-edge technology, but the technology alone doesn't guarantee compliance & that timelines are met. Efficient processes combined with technology does. As software and related service solutions become “commodities” in the daily business, Life Sciences organisations require effective and secure solutions, that are compatible with their requirements and deliver results. As a solution provider, PharmaLex, in collaboration with DocShifter, helps to drive compliance while improving the efficiency of the publishing processes. This is the start of the PharmaLex and DocShifter journey together, so listen to speakers from both organisations explain their exciting plans for the future.

Key learning objectives:

  • Discover how to implement a proven document conversion and validation solution for pharmaceutical, biotech and medical device companies
  • Learn about the software that automates, accelerates and simplifies the way to create submission-ready PDFs from original source documents; no matter which system these documents reside in
  • Enrich your knowledge on how to streamline the eCTD publishing process, from the technological and workflow perspectives
Download The free eBook