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StartingPoint submission authoring suite

A head start for pharma and biotech submissions

Making submission authoring simple

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.

Connect with us

New Customers

Contact Kim Lott
+1 913-319-1259

StartingPoint customers

If you’re an existing customer and have product questions or need details on StartingPoint.


Research and Development

We help reimagine R&D for pharma, bio and MedTech companies in a world that values patient outcomes.

Life Sciences

Combining new science with leading-edge technology to help companies deliver better patient outcomes.

Medical Technology

Working with Medical Technology companies to develop solutions across the patient’s entire healthcare journey.

Our leaders

Danielle N. Venice

Lead – StartingPoint Software Product