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Life Sciences

StartingPoint submission authoring suite

Helping pharmaceutical and biotech companies enable greater speed and efficiency in eCTD authoring, reviewing and publishing submission documents.

A head start for pharma and biotech submissions

Accenture’s proprietary platform, designed to streamline the e-invoicing process while maintaining compliance.

Making submission authoring simple

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.

  • Drug and device templates: 450+ Common Technical Document (CTD) and 100+ medical device templates.

  • Microsoft compliance: Custom toolbar integrated into Microsoft Word.

  • CTD specific design: Predefined heading styles, fonts, margins and table formats.

  • Pre-set validation and compliance: Advanced document validation, Physician Labelling Rule (PLR) functionality, and reference management and 100+ medical device templates.

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Our leader

Danielle N. Venice

Lead – StartingPoint Software Product

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