Standardized Reporting Structure:
Streamline internal reviews and regulatory submissions with consistent, professional formats.
Centralized Sources. Rapid Reporting. Exceptional Accuracy.
Faster to write. Faster to review. That’s the ROI.
From regulatory submissions to clinical trial reports, CITE accelerates the entire research reporting process by centralizing clinical data, QA/QC records, safety assessments, and audit submissions into a unified workspace. The report and its sources stay connected from the first draft through review. A short pilot on a few real reports will show the time save.
Eliminate fragmented workflows. No more manual evidence searches, formatting references, or assembling exhibits by hand. CITE’s integrated experience keeps your team focused on quality content—not on tedious processes.
CITE isn’t merely a citation tool—it’s a comprehensive report creation platform for pharmaceutical and clinical research needs. Use customizable templates for regulatory submissions, clinical study reports, safety evaluations, QA/QC documentation, and audits. Enjoy familiar Word-style editing tailored to regulatory, clinical, and compliance teams.
Instantly generate interactive PDFs containing your report, embedded citations, and clickable source files in a single file—no manual document assembly required.
End the last-minute scramble before audits or regulatory submissions. CITE maintains continuous links between citations and underlying sources, keeping your team prepared for compliance checks and audits at any time.
Free your team from version control and citation formatting. Allocate more resources toward clinical innovation, refining safety monitoring, enhancing quality assurance, or proactively managing regulatory changes.
We offer a free pilot for organizations that want to run CITE on their own submissions. Three to five source-intensive reports will show what faster writing and faster review are worth.
Easy Integration and Deployment
Works Seamlessly with Your Current Tools
CITE integrates effortlessly into your existing technology stack—including SharePoint, clinical data systems, and custom regulatory compliance solutions—without requiring extensive migrations or complex integrations.
- Convert 100+ file formats easily; upload clinical data, trial documents, regulatory guidance, and supporting evidence quickly
- Full offline capabilities, ideal for field teams or clinical trial managers
- Built-in audit logs and time-stamped citations ensure defensibility and compliance
- Export comprehensive interactive PDFs suitable for regulators, auditors, and stakeholders
Built for Clinical Research Documentation
Aligned Teams. Unified Workflows. Clear Handoffs.
Whether managing clinical trials, regulatory submissions, safety reports, or audits, CITE ensures your teams consistently deliver precise, efficient, and audit-ready documentation.
Custom Templates and Source Control
Utilize shared templates for submissions, reports, or safety assessments, maintaining centralized, version-controlled sources.
Instant Continuity
Facilitate seamless transitions across teams, ensuring clarity in logic, sources, and conclusions without rework.
Cross-Team Collaboration
Simplify multi-department or multi-site cooperation using interactive PDFs.
Frequently Asked Questions
CITE is Windows desktop software you install locally. Download the free trial, then run CiteSetup.msi. When you first launch CITE, you can set up your license in the app—choose a free trial or a paid plan. You do not have to activate a license before you open CITE.
Create or open a project (.cit file) and import supporting documents. Open those files in the Viewer, then create citations to them in the report editor. When you are ready, export a linked interactive PDF for reviewers.
Want a walkthrough first? Book a demo through the contact form. Enterprise customers can add dedicated onboarding and customized training.
Most users are up and running in under 30 minutes. CITE’s interface is intentionally designed to feel familiar to anyone who’s used Microsoft Word. Enterprise licenses include personalized onboarding sessions, group training, and a dedicated account manager to help configure workflows and templates.
Yes. CITE runs locally, supports full audit trails, and uses time-stamped citation tracking for defensibility.
Absolutely. Use firm-specific templates for filings, risk reports, or exam responses. Custom citation styles supported.
Yes. Export an interactive PDF they can open with any standard PDF reader—citations and sources included.
Optionally. CITE does not require AI. If you connect a verified provider (ChatGPT or Gemini—using your account/API arrangement), you can use assisted actions such as summarize, rewrite, or extract key points on text you choose to send. That transmission goes to the provider you selected under that provider’s terms; it does not go to an in8development-hosted model. Do not connect AI, or send source material, unless that provider meets your security obligations. See Security for the shared-responsibility summary.