Document Audit for Life Sciences
Remove Risk Elements & Ensure Style Compliance
Before accepting documents from an outside source and in advance of providing documents to another business unit, to a regulatory body or a publication, consider using the Microsystems Document Audit Service to avoid downstream document issues.
When to use a Document Audit:
- Before Publishing
- Analyze submission documents in advance of rendering
- Identify risky information in papers targeted for publication in medical journals
- Utilizing outside medical writing resources
- Assess documents received from contract writers to ensure alignment with your QC checklist
- Collaborating with a partner for the marketing, submission approval of a drug
- Internal document QA—analyze documents before sending them to a partner, and analyze the partner's documents before saving them into the DMS
- Consolidating documents after a merger/acquisition
- Identify risk elements—analyze a collection of documents that is received as part of a merger
- Consolidate templates—determine whether a collection of documents can be moved to a single template
- Consolidate technologies—use solutions to change templates if differences exist
- Migrating to a newer version of Microsoft Office
- Updates/migration of existing templates
- In process documents
A Microsystems Document Audit can help you:
- Avoid submission delays due to document non-compliance
- Understand issues either in templates or legacy documents that may arise when migrating to Office 2007 or 2010
- Avoid embarrassment and/or risk tied to hidden comments being published in documents
- Push back on outside authoring resources to fix non-compliant documents; reinforce document standards with outside resources
Learn more about how the Document Audit Service Works
Consult with us about your current situation and your need for a Document Audit, please
or call 630.598.1100.
