Translation & Redaction - AI applied in Regulatory Content Preparation
For those that wonder how submissions were done before eCTD. This was 2007. Some of us are old enough to remember. :-)
And we are possibly already moving into a new era with the AI use cases. And AI is offering huge opportunities for faster and more efficient content preparation.
Is document translation and redaction taking too much of your time? Why not simplify your content preparation with AI?
Are your documents stored in Ennov, Veeva, SharePoint, Documentum, CARA, Docubridge or any other content management system? Leverage automation to make this cumbersome process a breeze.
How?
Discover more in our webinar on November 7.
Who should attend?
Clinical Data/Data Managers
Clinical Operations and Processes
Contract Research and Service Support Providers
Document and Records Management/Specialists
Emerging Pharmaceutical/Biotech/Device Professionals
Essential Document Process and Business System Owners
Informatics/Bioinformatics Professionals
Information Technology and Support Personnel
Medical, Technical, and Regulatory Writers
Outsourcing/Clinical Outsourcing
Quality Assurance/Quality Control and Compliance Professionals
Quality Management
Regulatory Affairs and Operations
Regulatory Informatics
Regulatory Information Management
Regulatory Standards Implementation Specialists and Associates
Strategic Planning and Operations
Submissions and Global Submissions Management/Project Management
TMF and eTMF Management
Vendor Relationship Managers