Conference Description:

Who Should Attend:

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