Confidence Beyond Compliance

Preparing and generating FDA-compliant reports for Method Validation, Method Transfer and Product Stability can be a time-consuming and difficult exercise.

PharmaLex software is a complete solution for a more streamlined and productive laboratory.

The benefits:

  • Fully validated: Our software is 21 CFR part 11 and GAMP 5 validated.
  • Regulatory Friendly: Our software is compliant with global regulatory standards, including: ICH, EP and USP.
  • Software-as-a-Service: Access the software via the Internet. All upgrades and maintenance are handled by our administrators and published worldwide.
  • Safe Data: Complete encryption, Safely delete all private data from our server data at log-out
  • User friendly: Generate your report in less than 10 minutes!
  • Focused on decision-making: Extensive use of graphs and charts enhances the decision making process.

For more information on our software solutions, please contact us on contact@pharmalex.com.

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