StartingPoint submission authoring suite
Helping pharmaceutical and biotech companies enable greater speed and efficiency in eCTD authoring, reviewing and publishing submission documents.
StartingPoint allows rapid deployment of authoring standards across all functional areas to facilitate efficient formation of submission documents.
Learn how our industry-leading submission authoring solution facilitates efficient creation of submission-ready regulatory documents compliant with International Conference on Harmonization (ICH) and regional structure and formatting requirements.
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 and 100+ medical device templates.