21 April 2022, Thursday, between 17:00 – 17:30 CET
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.
Today, many Life Sciences companies still struggle with their submission content preparation; manual steps involved introduce risks and slow down submissions.
Fully automating your content preparation for regulatory submissions is possible.
Join our webinar, and discover how you can accelerate your submission content preparation.
Jennie May, Director, Regulatory Informatics and Operations at PharmaLex, a global solution provider, will also explain how they have simplified this process at PharmaLex for their global customers.
Key Learnings
- 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
