Data is spread across sources.
EDC, labs, safety, and vendor outputs tell different parts of the story.
Bring the study into view →For pharmaceutical & biotechnology teams
Your study is connected.
Your review should be, too.
Bring clinical data, study documents, and the evidence behind your findings into focus.
Clinical data consulting, CRO oversight, and in-house DM expertise—alongside ClinDRA™ and ClinDOC™ review tools.
25+ years of clinical data experienceTwo flagship products used by customersConfigured & supported around your study
Where review breaks down
The information exists.
Getting to the answer takes too much work.
An amendment changes more than the protocol.
Which plans still reflect the old requirements—and where?
Trace document impact →Updates depend on manual assembly.
Teams need current review priorities and useful outputs for their next discussion.
Build a repeatable workflow →Clinical data consulting
Experienced support for the work
your team is accountable for.
Bring Arclium into your study team for a focused need or ongoing clinical data management support. Consulting is available independently of ClinDRA and ClinDOC.
CRO & vendor oversight
- Review deliverables, progress, and open issues.
- Challenge gaps and escalate risks with context.
- Track actions with your CRO and internal team.
In-house DM expertise
- Add experienced clinical data management capacity.
- Support study decisions and cross-functional coordination.
- Translate data issues into clear priorities.
Study delivery support
- Review CRFs, EDC requirements, and study plans.
- Support queries, coding, and data reconciliation.
- Prepare for database lock and key milestones.
Two products. Complementary review workflows.
Understand the data.
Keep the documents aligned.
Clinical data review
ClinDRA™
Clinical Data Review Assistant
- Connect study data in a consistent review workspace.
- Investigate subject profiles, trends, and review flags.
- Use defined checks and programs; AI is optional.
Protocol-driven document review
ClinDOC™
Clinical Document Optimization Consultant
- Review supporting documents against the protocol.
- Investigate potential gaps and amendment impact.
- Trace requirements to document evidence before deciding.
A partner in the work
Built around your study.
Supported as it evolves.
- Study-specific sources, checks, views, and outputs.
- Deployment and data access agreed with your organization.
- Human review and approval points where you want them.
- Ongoing support for new sources, amendments, and review needs.
Start with your study
Show us where review
gets difficult.
Let’s discuss the expertise, review tools, or ongoing support your team needs.