Life Sciences Solutions — SharePoint 21 CFR Part 11 Compliance
NextDocs Document and Quality Management software helps pharmaceutical companies efficiently produce a safe, reliable, and effective drug while maintaining compliance with GxP regulatory requirements, and reducing the time to market and costs.
NextDocs streamlines inefficient, paper-based systems to shorten time to market and mitigate risks. By automating routing SOPs, DHF, DMR, and other documentation; obtaining approval and signatures; and manual search and retrieval of documents during FDA inspections, NextDocs ensures compliance, increases efficiency and reduces costs.
NextDocs connects various quality management processes, reduces cost of validation by automating labor-intensive validation tests conducted by internal staff and helps reduce exorbitant consultant fees which can easily double a company’s compliance costs.
Solutions for Pharmaceuticals, CRO’s, Medical Devices and BIO tech industries are readily available including:
• Clinical Trial Document Management
• SOP & Employee Record Document Management
• Quality Management
• Regulatory Document Management
• Project Document Management
• Document Management
• Marketing Management
Manufacturing Industry Solutions
NextDocs provides centralized and consolidated tracking, workflow management, and reporting for all critical business processes. NextDocs helps manufacturers minimize downtime, reduce scrap and meet customer expectations in a cost-effective manner. Solutions include…
Other ideal industries include…
• Energy & Utilities
• Food & Beverage
• Consumer Packaged Goods
• Chemical
• Automotive
• Aerospace & Defense
• Financial Services
• Government
• Military
• Oil & Gas