TMF Plus and eCTD Plus 2018

TMF Plus and eCTD Plus 2018 is a workshop that covers topics such as:

• ECTD Plus
  • Standard Operating Practices
  • Electronic Common Technical Document (eCTD)
  • Outsourcing
  • Regulatory Operations Tools of the Trade
• TMF Plus
  • Record Retention
  • Essential Documents
  • Document Archival
  • Regulatory Inspections
  • Document Destruction

TMF Plus and eCTD Plus 2018 brings together:

• Personnel involved in set up, maintenance, and auditing of the Trial Master File
• Records Management Specialists at Sponsors, CROs, FSPs, Vendors, Clinical Sites
• Project and/or Clinical Trial Assistants
• Project and/or Study Managers
• Clinical Research Monitors
• Clinical Operations Administrators
• Compliance Auditors
• Quality Assurance Personnel
• ECTD Publishers and Content Providers at Sponsors, CROs, Service Providers, Software Providers
• Consultants working in the life science industry involved in managing regulated content
• Regulatory Affairs Professionals
• Regulatory Operations Personnel
• Professionals preparing eCTD Marketing Applications for any Global Adopting Agency
• Anyone new to the eCTD Delivery Paradigm
• Clinical Research Professionals
• Research and Development Professionals
• Submission Document Authors
• Medical and Technical Writers
• IT Professionals
• Project Managers