Document Management

Empower your organization with the SciCord Document Management solution. Enhance your documentation workflows, boost collaboration, and maintain complete control over versioning, approvals, and compliance.

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Balancing Lab Efficiency with IT and Compliance Requirements

Are you grappling with the complexities of document management, struggling to maintain version control, and ensure proper reviews and approvals? Does your current process hinder collaboration and transparency, putting compliance at risk?
Unlock a more efficient and streamlined approach to document management with the SciCord Document Management solution. Simplify your documentation workflows, enhance collaboration, and maintain complete control over versioning, approvals, and compliance.

Efficient Documentation Control

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.

Flexible Lifecycle Management

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.

Enhanced Collaboration

Assign one or more reviewers to documents that require additional scrutiny, fostering collaboration and ensuring the highest quality in your documentation.

Simplified Record Keeping

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.

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Document Identifier

Assign unique identifiers to each document, simplifying document tracking and retrieval.

Version Control

Manage both major and minor document versions, ensuring a clear and accurate record of document evolution.

Electronic Reviews and Approvals

Facilitate electronic reviews, approvals, and signatures within managed PDF documents, reducing manual processes and expediting document workflows.

Collaborative Workflow

Assign multiple reviewers to documents requiring additional scrutiny, enabling efficient collaboration and quality control.

Flexible Lifecycle Management

Define document lifecycles tailored to your specific needs, from one-analyst handling to multi-level reviews and final quality approvals.

Comprehensive Audit Trail

Maintain a complete history of document revisions, reviews, and approvals, ensuring transparency and compliance with regulatory requirements.

User-Friendly Interface

Utilize an intuitive interface that simplifies document creation, tracking, and management, promoting user adoption and productivity.


Trusted by organizations of all sizes



What Our Users Say


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.

“Not a day goes by where I don’t reflect on how much easier your system makes this job.”
“We have been audited by FDA twice and they had no concerns about the system nor any findings.”
– Deb Carr, Director, IPD
“The implementation was quite smooth. The team came onsite and worked in parallel with our IT team.”
“Really cool to have data and CofA in the same system. I’ve used other solutions which require access to multiple systems to get the full picture.”
– Radu Mihaila, Director CMC at GBT & Pfizer
“[After sales support is] consistently excellent. They respond quickly, investigate thoroughly, and they can explain everything in a way that we understand and can convey.”
“My experience with the entire team (US & Europe) has been amazing. They are just a phone call away. My work has never suffered because of the lack of the support from their team.”
-Indu Chowdhary, PhD
“In a head to head competition, SciCord was 3x more efficient at documenting a typical work process than [competition]. A complete ‘Assay’ work process required 60 minutes in [competition], while only 20 minutes in SciCord!”
“Very impressed with the Demo. We actually had a call with another vendor just after your demo and they didn’t have half of the capabilities that SciCord was able to show.”
“We can scale our production up to 40% thanks to [SciCord].”
“Other LIMS systems are more challenging to implement”
– Radu Mihaila, Director CMC at GBT & Pfizer


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Reach out to Schedule a Meeting and get more information about how SciCord can fit into your lab

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8601 Six Forks Road, Suite 400, Raleigh, NC 27615


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