Automating submission document preparation in OpenText Documentum with DocShifter (inc. practical demo)

​​Are you looking for ways to further automate and simplify the way you prepare content for submissions in OpenText Documentum?

​​​Combining the power of DocShifter with OpenText Documentum, 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 Virtual documents 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 September 28th. 

​​​* 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.

• ​​​OpenText Documentum customers benefit from using DocShifter

• ​​Metadata and document lifecycle management in OpenText Documentum 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