Operation System
HomeDiscoverInstrumentsOperation SystemApplicationsAccessoriesOrdering/TechnicalVIP 
 

  PC software epBlue GxP™  

epBlue GxP™ software is part of Eppendorf’s epMotion GxP solution including an automated pipetting system hardware, epBlue GxP software and certificates, plus dedicated certification and validation services. All available PC versions of epMotion are offered also as specific epMotion GxP solution versions.

Save time and gain certainty for your automated liquid handling

The new epMotion GxP solution was developed according to GAMP 5 and tailored for organizational and process requirements of 21 CFR part 11, 58, 211 and 820, GLP and GMP. Eppendorf has taken care of the major part of the required system validation and qualification, leaving users more time to focus on validating their application part.

Features of epMotion GxP Version:

  • Complete electronic documentation (application, log file, audit trail)
  • User level management & access control (Great flexibility with 5 levels: Admin, Admin Lab, User Level1, User Level2, Guest)
  • Audit trail & log file (Tracking & documentation of all user intervention and all actions of the processes on epMotion)
  • Configurable workflow management
  • Electronic signatures
  • Certification following industry standard algorithm
  • Export and archiving of digital signed documents
  • Data base system (for better data security & integrity)
  • ID tracking using barcodes (optional extension for simple communication with your LIMS and ELN)

epMotion GxP solution ordering:



Dedicated certification and validation services
Eppendorf offers global certification services in compliance with FDA 21 CFR Part 11, EU GMP Annex 11, GLP and GAMP 5 to facilitate your validation process. We support you with different certified qualification programs for your instrument, software and personnel.



Certified quality for your validation process
form external company that the epMotion GxP system fully complies with 21 CFR 11, 58, 211, 820 and was developed corresponding to the GAMP 5 standard.
- This document describes the technical implementation and the process-related implementation by work instructions or company policies of the requirements stipulated in the legal text of 21 CFR Part 11.

or

 
Manage
Bookmark and Share
Keyword
Catalog number
Find your certificate
Lot Number specific Certificates (Biopur®, PCR Clean & Sterile)
Lot No

General Quality, ISO and Dispensers Certificates