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
 
 
Zoom
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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