eGMP Enterprise Software
      Customizable Enterprise Data Tracking - Fast, Secure, Easy To Use - 415-531-6319
  • 21 CFR Part 11 Compliant
  • Web Enabled Workflow
  • Customizable, Use Any Data
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eGMP Customizable Enterprise Software
Track All Data, Lock Down, Web-Expose - 415.531.6319 - info@chemscope.com
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Welcome to eGMP, an integrated software solution that enables companies to create custom enterprise software on the fly. No programming required, no data conversion required! The eGMP software suite comes preconfigured with custom data table templates, and enables companies to manage ALL aspects of workflow, from traditional document control function like SOP, Specifications, Methods, Validation Reports, Qualification Protocols, and Design Reviews to time card management, procurement, inventory and more. eGMP has a complete security model built in, with provision for secure management of the core process of routing, tracing, and approval. Users also have the option of importing existing data tables (excel, lotus, text, etc), and organize by deparment. And eGMP is so flexible that companies can readily create their own tables with the click of a mouse. And since eGMP is XML compliant, business partners and existing solutions can readily be integrated online as well. Security? Security can be enforced at superadmin level, admin level, department level, user level, and file level with control over write, read, and no view. Finally, eGMP is compliant with FDA regulations, including 21 CFR Part 11. And all through a single web browser!

What eGMP Can Do
  • Use Any Data Source, AS-IS!
  • Create Custom Tables, Organize By Department
  • Track Training, Issues, Documents
  • Integrate Existing Office Docs
  • Reduce Costs/Acc. Development
  • Improve Regulatory Compliance
  • Manage Manufacturing Workflow
  • Integrate Data From Diverse Workflow
  • Security at Department and User File Level
  • Desktop Product Orders
  • Complete Data Management
cGMP Integration
  • Route, Trace, Audit, Approve
  • Qualification Prot. & Rprts.
  • Batch Records/Devtn Rpts.
  • Validation Prot. & Rprts.
  • PM & Calibration
  • cGMP Room Scheduling
  • Standard Operating Procedures
  • Raw Material Mthds./Specs.
  • Link Each File Up To 25 Others
  • Desktop Product Orders


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