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Implementing the Common Technical Document (CTD) Format for NDA Submissions
Who Should Attend
This introductory-level course is designed for those responsible for writing regulatory submissions within the Pharmaceutical and Biotechnology industries. Specifically, the following professionals would benefit most from the course:-
Regulatory Affairs Specialists/Associates
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Medical Writers
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Clinical Research Directors
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QA/QC Specialists
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Clinical/Preclinical Research Scientists
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Project Managers
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Documentation Specialists
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Technical Writers
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Consultants
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Drug Development Professionals
Booking Options
Booking Options:
- Register online or Call Customer Service - Tel: (866) 647-0921 or email register@pti-international.com
- Group Discounts (3 or more people for this course) - Call your Course Guidance Manager at (646) 895-7447 or email CourseManager@pti-international.com
- Bring this Course to Your Facility (10 or more people or further customization) - Call (800) 303-8194 or email OnSiteSolutions@pti-international.com