GLP Good Laboratory Practice

GLP certification ensuring reliability and reproducibility in chemical and biological product testing.

Standard
GLP
Edition
Validity
1 years
Surveillance
Annual surveillance audit

What is GLP?

GLP (Good Laboratory Practice) is a set of principles that ensures test studies in health and environmental safety are planned, performed, monitored, recorded, and reported in a reliable, transparent, and reproducible manner. Internationally recognized by the OECD, GLP is commonly required for chemical substance testing.

BESA Consulting Scope

  • Assessment of laboratory infrastructure against GLP principles
  • Development of Standard Operating Procedures (SOPs)
  • Personnel training and competency evaluation
  • Internal audit support for quality assurance units
  • Management of GLP compliance certificate application

Benefits

  • Easier data acceptance by OECD and EU regulatory bodies
  • Reliability and international validity of test results
  • Competitive advantage in chemical substance licensing processes

Certification Process

  1. 1 Application and scope definition
  2. 2 Gap analysis and documentation
  3. 3 System implementation and internal audit
  4. 4 Stage 1 and Stage 2 audit
  5. 5 Certificate issue
  6. 6 Annual surveillance and recertification

The certificate is issued by an accredited certification body; BESA manages the process from application to certificate.