Interested in learning more about Regulatory Medical Writing? There's an upcoming Regulatory Medical Writing Conference that you may want to attend. Here's what it's about:
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
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
The conference will run Sept 22-23 in Philadelphia. Learn more and register here.
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