Cover Image for How to render Veeva binders with DocShifter into submission-ready PDFs (and other content automation)

How to render Veeva binders with DocShifter into submission-ready PDFs (and other content automation)

Hosted by Geert Van Peteghem & Paul Ireland - VP Life Sciences
 
 
Virtual
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About Event

​Are you having troubles converting your Veeva binders into consolidated PDFs? And looking for ways to further automate and simplify the way you prepare content for submissions? 

​​Combining the power of DocShifter with Veeva, you can take submission content preparation to the next level. The automation allows you to focus on what matters most: the content. 

​​How will this powerful combination help you save time with the following?

  • ​​Rendering Veeva binders into consolidated, health authority compliant PDFs

  • ​Microsoft Word & PDF content preparation and validation

  • ​​Report generation

  • ​​Rendering documents to multiple health authority compliant PDFs simultaneously

​​Discover it all in our 30-minute webinar on August 31st. 

​​* Please make sure to register with your company email address!

​​Learning Objectives

​​See how you can easily leverage rendering technology for all your content stored in Veeva to fully automate and simplify the:

  • ​​Dull and costly QA / QC checks on Microsoft Word and PDF documents

  • ​​Complex report generation process, using report publishing tools

  • ​​Manual-intensive PDF content preparation process for one or more health authorities

​​This webinar will also give you the opportunity to understand how:

  • ​​DocShifter's content automation workflows strengthen Veeva to simplify and accelerate your submissions.

  • ​​Veeva customers benefit from using DocShifter

  • ​Metadata and document lifecycle management in Veeva can be used to trigger DocShifter's automated workflows

​​We look forward to seeing you in our webinar on August 31st, Thursday.

​​Who should attend?

  • ​​Regulatory Affairs and Operations

  • ​​Regulatory Information Management

  • ​​Submissions and Global Submissions

  • ​​Management/Project Management

  • ​​Medical, Technical, and Regulatory Writers

  • ​​Clinical Data/Data Managers

  • ​​Information Technology and Support Personnel

  • ​​Document and Records Management/Specialists

  • ​​Essential Document Process and Business System Owners

  • ​​Regulatory Standards Implementation Specialists and Associates

  • ​​Clinical Operations and Processes

  • ​​Quality Management

  • ​​Quality Assurance/Quality Control and Compliance Professionals

  • ​​Strategic Planning and Operations

  • ​​Contract Research and Service Support Providers

  • ​​Emerging Pharmaceutical/Biotech/Device Professionals