GLP Consultancy
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GLP (Good Laboratory Practice)
GLP consultancy
Sistem Patent Kalite provides Good Laboratory Practice (GLP) consultancy as an active service, led by specialists who work alongside the laboratory's own team. A typical GLP work plan covers five core areas:
- Quality management system optimisation and structure
- Quality documentation system optimisation and structure
- In-house GLP practice optimisation and structure
- Quality management aligned with current practice and OECD guidance
- Laboratory workload and workflow optimisation
Who benefits from GLP consultancy
Laboratories that carry out non-clinical safety studies on pharmaceuticals, agrochemicals, biocides, cosmetics, food additives, and industrial chemicals all operate under GLP expectations. For those laboratories, setting the system up correctly the first time saves significant cost at audit, especially if the work is meant to be used across borders.
How the consultancy runs
A project starts with a review of the laboratory's current workflows, documentation, and staff roles. Gaps against the GLP principles are identified and closed in a prioritised sequence. Internal audits and a management review round out the work before the laboratory applies for GLP compliance recognition from the national monitoring authority.
Why work with Sistem Patent Kalite
The team has hands-on experience with GLP projects and understands how the OECD principles read in the laboratory day to day. Clients receive a plan they can follow, along with the templates and guidance they need to run the system after the consultancy engagement ends.
