How to automate submission content preparation & report generation for content stored in Veeva
Are you using Veeva to store and manage your submission content?
The automation of regulatory content does not need to stop there.
Combined with the power of DocShifter, we can take automation to the next level. So you can focus on the content.
How will this powerful combination help you save time with the following?
Microsoft Word & PDF content preparation and validation
Report generation
Rendering Veeva binders
Rendering documents to multiple health authority compliant PDFs simultaneously
Discover it all in our 30-minute webinar on April 27th.
* 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 can strengthen Veeva to simplify and accelerate your submissions.
You can take automation to the next level in Veeva with DocShifter
We look forward to seeing you in our webinar on April 27, 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