GLP is an internationally recognized framework for good laboratory practice. It helps organizations translate policy commitments into controlled processes, measurable objectives and evidence of continual improvement.
Who should consider this program?
Testing facilities requiring consistent study planning, conduct, recording and reporting.
Business outcomes
- Improve study integrity and traceability
- Clarify roles and quality assurance
- Control equipment, methods and records
- Strengthen defensibility of results
How the assessment works
Application
We review activities, locations, personnel, requested scope and applicable requirements.
Planning
The responsible body, assessment method, timing and commercial conditions are documented.
Evaluation
Qualified personnel evaluate implementation using interviews, records, observation and sampling.
Independent review
Findings and corrective actions are reviewed before the applicable decision or statement is issued.
Preparing your organization
Define the intended scope, identify applicable legal and customer requirements, assign process ownership, maintain documented information and complete an internal review before the formal assessment. The duration depends on organization size, complexity, locations, shifts, risk and readiness.
Related frameworks
Frequently asked questions
Discuss GLP with our team
Receive a proposal based on your organization, locations and intended certification or assessment scope.