Regulatory Medical Writing Conference

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The only event that deals constructively with core issues of
document review and compiling information for document authoring.

  • Uncover innovative strategies to streamline the document review process
  • Learn how the medical writing department is being consolidated and reorganized to address new challenges in the regional and global submissions processes
  • Bridge the gap of divergent information systems and uncover gaps in the development process early enough to correct them
  • Reduce the number of drafts necessary to form your final submissions document
  • Maximize your time to respond to regulatory inquiries by evaluating the document life cycle


Register today and join us as we tackle, head on,
some of the critical issues facing the regulatory writing process today.



Who Should Attend

 

Professionals from Pharmaceutical, Biotechnology and
Medical Device companies with responsibilities in the following areas:
  • Regulatory Medical Writing
  • Submissions Management
  • Scientific Communications
  • Technical Writing
  • Regulatory Affairs
  • Scientific Information
  • Clinical Research
  • Regulatory Operations
  • Data Management
  • Document Management
  • Electronic Submissions
  • Clinical Operations
  • Project Management
  • Regulatory Publishing

 

This conference is also of interest to:

  • Document Application Suppliers
  • Information Management Consultants
  • Research Informatics
  • CROs providing content management
  • Medical Writing Services
  • Bibliographic Software Suppliers
  • Clinical Research Organizations

 

If you have any questions about this event please feel free to contact us at 866-207-6528 or email the conference director, Terry di Paolo.