search
close_mark

How the Integrated Search Workflow in CAPTIS® Is Transforming Literature Reviews for Regulatory Teams

How the Integrated Search Workflow in CAPTIS® Is Transforming Literature Reviews for Regulatory Teams

13 Aug, 2025

At Celegence, we know that efficiency, consistency, and traceability are critical when preparing regulatory documents like Clinical Evaluation Reports (CERs). That’s why we’ve adopted and optimized the Integrated Database Search workflow in CAPTIS®, our go-to solution for systematic literature reviews.

This powerful feature allows our medical writers to search PubMed, Europe PMC, and Google Scholar directly within the platform, replacing the need for manually compiling article data in Excel. By eliminating export-import steps and disconnected tracking, it makes literature reviews significantly faster, cleaner, and fully audit-ready.

These integrated searches were among the first features we prioritized when designing our automated literature workflow, because anyone who has reviewed from spreadsheets knows how time-consuming it is to collate article data, especially from sources like Google Scholar. In fact, many manufacturers still outsource this step because of how tedious and error-prone it can be.

What Makes It So Effective?

  • All-in-One Search Access

    Our writers can search across major scientific databases (PubMed, EU PMC, Google Scholar) without leaving the platform. That means fewer clicks, less toggling, and no time wasted.

  • Smart Review Alignment

    Each search can be clearly tagged as part of either the DUE (Device Under Evaluation) or SOTA (State of the Art) workflow. This ensures that literature stays aligned with project goals and regulatory requirements from the start.

  • Built-in Relevance Indicators

    To quickly assess search quality, our teams use positive and negative keywords—a simple but powerful way to check if a search is pulling in the right kind of articles. It helps us know instantly whether a query needs fine-tuning, without wasting review time.

  • Audit-Ready Traceability

    Naming searches and maintaining search categories ensures long-term traceability — a huge benefit during regulatory audits or CER updates 2–5 years down the line. This also helps teams align on the overall literature review objectives in the project.

  • Search Editing Without Rework

    Need to tweak your search terms or expand a date range mid-project? No problem. You can edit a saved search, rerun it, and retain all previous screening decisions for overlapping articles. No duplication. No data loss.

  • Auto-Update for Long-Term Projects

    With Auto-Update enabled, the system will automatically refresh your search results weekly or monthly, capturing new publications as they appear — ideal for projects with rolling deadlines or submissions scheduled months ahead.

  • Rapid Reuse Across Projects

    Project cloning combined with search editing lets our team quickly reuse earlier searches — whether it’s extending the date range for a maintenance CER, swapping out key terms to adapt the search for a different device, or reusing the same SOTA strategy across multiple devices. It saves time, ensures consistency, and reduces rework across projects.

“We’ve seen measurable time savings and a more focused authoring and review process since adopting this workflow. Our literature teams are not only working faster and more efficiently, but their output is also far less error-prone and more consistently aligned with regulatory expectations. This ultimately strengthens the quality and reliability of our submissions.”

— Dr. Pratibha Mishra, Senior Manager and SME, Medical Device Services

Ready to Work Smarter With Literature Reviews?

This is just one example of how we’ve optimized regulatory work using CAPTIS®. If your teams handle CERs, PERs, or other evidence-based submissions, the right technology can dramatically simplify your workflows.

Get in touch  @ info@celegence.com to see how we can help you scale literature reviews without scaling your headcount.

 

AUTHORED BY

author-image

Technical Account Manager

Shruti Sharma

Linkdin-image

Shruti Sharma is a Technical Account Manager at Celegence with a deep background in regulatory medical writing, specializing in EU MDR-compliant clinical evaluations for medical devices. Drawing on her extensive knowledge of regulatory requirements, she translates industry needs into innovative software solutions that enhance efficiency and compliance in the Life Sciences regulatory space. Shruti is passionate about making technology accessible and impactful, championing tech-enabled process.

Other Related Articles

View All