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Traceable, Tamper-Proof Test Results in Accordance with FDA 21 CFR Part 11

Traceable manipulation-proof test results
  • Ever-increasing demands are placed on software used in the medical and pharmaceutical industries to document the traceability of completed actions.
  • With the traceability option, testXpert III enables logging of all actions and changes before, during and after the test, making test results and the documentation traceable and protecting them from manipulation.
  • Integrated user management and functions such as electronic records and electronic signature ensure that test results are always protected from tampering.
  • Together with the organizational measures and procedure instructions that apply to the individual companies themselves, the requirements of FDA in 21 CFR Part 11 are fulfilled.
  • ZwickRoell also offers a qualification service package (DQ/IQ/OQ) for validation support.
  • testXpert III logs all test and system related actions and settings and can therefore always answer the question

"When does who do what, why and who is responsible?" 

Traceable, Tamper-Proof Test Results in Accordance with FDA 21 CFR Part 11

testXpert III always knows  "When does who do what, why and who is responsible?" 

Safety-critical tests

The expanded traceability option can be configured as needed, and the degree of traceability can be defined. The administrator defines what must be logged and for which activities and events the user must enter a reason. In this manner, testXpert III offers the possibility of being individually adapted to the customer's QS regulations.

Electronic records

The Electronic Records function enables complete, tamper-proof documentation of all actions and changes performed in testXpert III. Users define the degree to which the actions must be logged and possibly explained in accordance with their regulatory requirements (for example, changes to a test-relevant parameter such as test speed). This data is stored in the audit trail.

  • The logging entries are saved automatically and independently from the type in the system audit trail or in the respective test programs/series.
  • The data is saved in binary coding and cannot be edited with Windows standard programs.
  • Output can be generated in "readable" form (HTML / PDF) anytime in testXpert III.
  • Logged data is archived in encrypted form.
  • The optional reason is automatically added to the respective report input (with the old and the modified value).
  • Comments can be inserted in the audit trail via a menu item.

Electronic signature

The electronic signature function also protects the test program/test series reliably from unwanted changes. It makes it possible to document who is assuming responsibility and at the same time, makes the audit trail paperless. The signature on the test report can be replaced by the test program/test series digital signature by entering the user name and password in the software, and it is possible to define how many people must sign and who has authorization to do so. Once signed, the test program and test series are protected from unauthorized changes.

Guidelines for the regulated areas of the medical and pharmaceutical industry

The regulation 21 CFR Part 11(Code of Federal Regulations) on electronic records and electronic signatures of the United States Food and Drug Administration (FDA) defines acceptance criteria for the use of electronic records and electronic signatures in place of records in paper form and handwritten signatures on paper. These electronic documents must be handled with as much confidentiality, be just as authoritative, and hold the same value as the paper documents.
Compliance with regulations FDA 21 CFR Part 11 and EU GMP guidelines Annex 11 on is required for use with electronic records and signatures in a regulated environment. It is still possible to use conventional paper documents and handwritten signatures.

Qualification of materials testing machines and instruments

A significant element of process validation in the medical engineering and pharmaceutical industries is the technical review of individual plant and devices. This qualification is also required for ZwickRoell materials testing systems used in the medical and pharmaceutical industry, because systems are subject to various legal requirements (for example, under Medical Devices Directive 93/42/EEC or regulations such as FDA 21 CFR Part 11).

ZwickRoell supports the qualification of materials testing systems in the DQ (design qualification), IQ (installation qualification), and OQ (operational qualification) processes by offering comprehensive and, if requested, individually tailored qualification documentation, as well as in the practical performance of qualification on site.

DQ IQ OQ qualification service

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testXpert III

Intuitive and workflow-based right from the start
testXpert III is the result of close cooperation with software users in the materials testing industry and the experience of over 40,000 successful testXpert installations. From the very start, testXpert III uses a workflow that is based on your lab processes to guide you step by step through your test. Get to know testXpert III and experience how easy it is to use.
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Getting started is easy!

The clear, logically structured workflow of testXpert III guides the operator all the way through test preparation, performance and results analysis. testXpert III is a workflow-based software that keeps training time to a minimum.
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One of the most reliable testing systems on the market

Unique System Configuration Builder
The unique System Configuration Builder makes it possible to define reproducible test conditions and offers maximum safety for the user and testing system. testXpert III always knows HOW, WHERE and WITH WHAT to test!
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The intelligent test configuration wizard

All test-relevant settings can be made using the intelligent wizard. The wizard shows the user which test parameters must still be configured and checks all entries for plausibility.
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