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StartingPoint submission authoring suite
Helping pharmaceutical and biotech companies enable greater speed and efficiency in authoring, reviewing and publishing submission documents
What's
In It
StartingPoint Submission Authoring Templates facilitate efficient creation of submission-ready regulatory documents compliant with International Conference on Harmonisation (ICH) and regional structure and formatting requirements. The StartingPoint content templates contain styles and macros to administer standards, avoid formatting issues and remove ambiguity from guidance.
450+ Common Technical Document (CTD) and 100+ medical device templates
Custom toolbar integrated into Microsoft Word
Predefined heading styles, fonts, margins and table formats
Advanced document validation, Physician Labelling Rule (PLR) functionality, and reference management
Contact
Us
StartingPoint Customers -
If you’re an existing customer and have product questions or need details on StartingPoint updates, please contact us at StartingPoint support
Non-customers and general StartingPoint information:
•US
913 319 1259
•Outside US
+44 (0) 203 626 1979
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With Us
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