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GLP Compliant Laboratory Setup: A Step-by-Step Guide to Success

What are Good Laboratory Practices?

GLP Compliant Laboratory Setup: A Step-by-Step Guide to Success

Good Laboratory Practices

GLP (Good Laboratory Practices) ensures that laboratories are set up and managed in accordance with certain standards to ensure reliable and quality results. Establishing a GLP-compliant laboratory allows you to work with internationally recognized methods while improving the accuracy of tests. Here are the steps you need to follow to set up a GLP compliant laboratory:

1. Planning the Laboratory Space

The first step in setting up a GLP-compliant laboratory is careful planning of the space. Laboratory space should be divided into sections according to the type of work and each section should be organized according to different functions.

  • Chemical analysis department
  • Microbiological testing area
  • Storage and logistics areas

Proper planning reduces the risk of errors in testing processes and ensures a more efficient workflow.

2. Equipment Selection in Compliance with GLP Standards

It is critical that the equipment used in the laboratory setup complies with GLP standards. High-precision instruments ensure reliable results.

  • Chromatography equipment
  • Pipettes and precision measuring instruments
  • Tools to support calibration and validation processes

Regular maintenance and calibration of equipment is a key requirement of GLP standards.

3. Personnel Training and Certification

Only physical infrastructure is not sufficient for a GLP compliant laboratory. Laboratory personnel must be trained and certified on GLP standards. Personnel:

  • Operation in accordance with test protocols,
  • Good command of the documentation process,
  • It is important to know the audit and reporting processes.


4. Documentation and Record Keeping

A key element of GLP is the detailed documentation of all processes. Each test step, the methods used and the results obtained must be accurately recorded.

  • Test procedures (SOPs)
  • Calibration and validation reports
  • Sample records

This documentation increases the transparency and credibility of your laboratory in audit processes.

5. GLP Compliant Testing and Quality Control

One of the main functions of GLP laboratories is to guarantee the reliability of tests. Quality control processes improve the accuracy of results by detecting potential errors. The following factors should be considered in GLP-compliant tests:

  • Repeatability
  • Sensitivity
  • Measurement accuracy

Following international methods and standards in testing processes ensures global acceptance of test results.

6. Audits and Continuous Improvement

Even after establishing a GLP compliant laboratory, it is important to conduct regular audits and improve processes.

  • Periodic internal audits
  • Preparation for external audits
  • Integration of new technologies and methods

Actions taken according to audit results support the continuous development of the laboratory.

Nano-lab Laboratories Group continues to provide services within the scope of GLP studies. We also provide services in Medical Device Analysis.

Contact us for more information.

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