Document Control Built for Labs — Without the Complexity
SciCord gives you the essential tools for versioning, approvals, and compliant document workflows, plus seamless integration points if you need a full Document Management System. Start managing lab documents immediately—and grow into a complete solution as your needs evolve.
Every lab knows the pain: dozens of SOPs, multiple versions floating around, reviewers on vacation, and the sudden panic when an auditor shows up. Managing documents in a regulated environment shouldn’t feel this chaotic.
If you’re dealing with scattered files, unclear version histories, or review processes that slow your team down—or leave compliance gaps—it’s time for a smarter approach.
SciCord delivers the essential document control tools labs need right away: structured versioning, clear review and approval workflows, and built-in transparency for teams and auditors. And when your organization requires more, SciCord integrates seamlessly with full Document Management Systems.
Purpose-built document management that makes compliance simple, collaboration fast, and science unstoppable.
Streamline the creation, revision, and management of related documentation. Ensure every document has a unique identifier, major and minor version control, electronic reviews, approvals, and signatures published within managed PDFs.
Tailor the lifecycle of index documents to suit your specific needs. From swift one-analyst completion for informal documents like method development to multi-level reviews and final quality approvals for critical documents, our solution adapts to your workflow.
Assign one or more reviewers to documents that require additional scrutiny, fostering collaboration and ensuring the highest quality in your documentation.
Easily maintain a comprehensive history of document revisions, reviews, and approvals, ensuring full traceability and compliance.
Electronic record and signature capabilities meet regulatory requirements, such as FDA’s 21 CFR Part 11. Detailed audit trails provide a complete history of all actions and are valuable for regulatory reviews and investigations.
Assign unique identifiers to each document, simplifying document tracking and retrieval.
Manage both major and minor document versions, ensuring a clear and accurate record of document evolution.
Utilize an intuitive spreadsheet based interface that simplifies document creation, tracking, and management, promoting user adoption and productivity.
Facilitate electronic reviews, approvals, and signatures within managed PDF documents, reducing manual processes and expediting document workflows.
Assign multiple reviewers to documents requiring additional scrutiny, enabling efficient collaboration and quality control.
Define document lifecycles tailored to your specific needs, from one-analyst handling to multi-level reviews and final quality approvals.
Maintain a complete history of document revisions, reviews, and approvals, ensuring transparency and compliance with regulatory requirements.
Reach out to Schedule a Meeting and get more information about how SciCord can fit into your lab
Don’t take our word for it.
We exceed our client’s demands everyday to make their research and discovery process simpler and more efficient.
This is by far the best value in science software (or anything else in science, really) that we’ve ever experienced. Other solutions in this price range had a fraction of the features, and those with the features cost 3x – 10x more. We’re very happy customers.
Josh Guyer,
Senior Pharmaceutical Scientist
SCIENTIFIC RECORDING
info@scicord.com
8601 Six Forks Road, Suite 400, Raleigh, NC 27615
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