Industries

The NextDocs Quality and Document Management Systems are the perfect solution for highly regulated businesses, such as pharmaceutical, medical device, biotechnology and contract research organizations.

Pharmaceutical
NextDocs enables businesses in regulated industries to comply with FDA and ISO regulations and ever-evolving standards—while at the same time automating processes, improving efficiency and dramatically reducing costs. NextDocs is the leader in SharePoint-based regulatory document management solutions including FDA 21 CFR Part 11.
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Medical Device
The Medical Device Industry is faced with various regulatory compliance and time to market challenges. NextDocs’ out of the box solutions for the medical device manufacturers enables them to achieve full compliance, reduce manual operations, and streamline reporting while improving profitability.
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Biotech
NextDocs understands the challenges faced by Biotech companies and provides an integrated quality management system that builds compliance and quality into existing SharePoint based business systems.
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Clinical Research Organizations
At NextDocs, our focus is on addressing the needs of life sciences companies. We understand the special requirements of pharmaceutical, medical device, biotechnology and contract research companies that operate in a highly regulated environment.
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Beyond Life Sciences
NextDocs provides centralized and consolidated tracking, workflow management, and reporting for critical business processes. While initial adoption has been primarily in life sciences companies, the capabilities in the NextDocs software suite are readily adaptable to other industries such as manufacturing that must address regulatory requirements or industry standards for managing documents, such as ISO 9000.
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NextDocs Compliance Platform

The NextDocs Document and Quality Management systems are built on the NextDocs Compliance Platform which addresses the entire range of 21 CFR Part 11 requirements.

Features include:: PDF Rendering; Overlay; Watermark; Lifecycle management; Version tracking; Audit trials; Check In/Check Out; Document numbering; Adobe PDF conversion; Digital/E- signatures; Metadata tagging; Folder templates; Watermarks & overlays

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