Clear responsibilities
Study directors, principal investigators, quality assurance and technical staff understand their roles.
Good Laboratory Practice Implementation
Build a GLP system that protects the integrity of your studies.
Reliable study data depends on controlled planning, clear responsibilities, traceable records and independent quality assurance. We help laboratories translate Good Laboratory Practice requirements into practical systems that staff can follow and management can monitor.
GLP is about trustworthy studies, not paperwork alone.
A strong GLP system connects the study plan, personnel, equipment, test systems, raw data, quality assurance and final report. We help you build these controls around the way your laboratory conducts studies.
Controlled study records
Raw data, deviations, changes and approvals are documented and traceable.
Secure retention and archives
Study materials and records are stored, protected and retrievable for the required period.
What our GLP implementation support can include.
Your project can begin with a gap assessment or extend to complete implementation and readiness support.
GLP Gap AssessmentReview current practices, study controls, documents and facilities.
Policies, SOPs and FormsDevelop practical documents for study conduct, records and quality assurance.
Study Planning and ControlStudy plans, amendments, responsibilities, deviations and final reports.
Equipment and Facility ControlsMaintenance, calibration, environmental conditions and suitability.
Test and Reference Item ManagementReceipt, characterisation, storage, distribution and accountability.
Quality Assurance ProgrammeStudy audits, facility inspections, reporting and follow-up.
A practical four-step implementation process.
1
Assess current practices
We review facilities, study controls, personnel, records and quality assurance activities.
2
Build the system
Required policies, procedures, forms and responsibilities are developed or improved.
3
Train and implement
Staff are guided through the new controls using practical examples from their work.
4
Audit and improve
Implementation is reviewed, gaps are corrected and readiness is reassessed.
3–9 months
Focused assessments are faster. Full implementation depends on laboratory size, study complexity and staff involvement.
From ₦400,000
Final pricing depends on scope, number of studies, documentation needs, training, site visits and quality-assurance support.
Frequently asked questions.
GLP support is especially useful for non-clinical research, toxicology, environmental studies, pharmaceutical development, contract research and laboratories generating data for regulatory or commercial decisions.
Yes. We can begin with a gap assessment, define the required system and support documentation, training, study controls, quality assurance and implementation.
No. They overlap in areas such as personnel, equipment, records and quality control, but they serve different purposes. GLP focuses strongly on the organisation and conduct of non-clinical studies, while ISO 17025 focuses on laboratory competence for testing and calibration.
Yes. We can review study plans, raw data, equipment records, test-item control, deviations, archives and final reports against the agreed GLP requirements.
A focused assessment may take one to three weeks. Full implementation often takes three to nine months, depending on laboratory size, study complexity, documentation maturity and staff availability.
Tell us about your GLP project.
Share your laboratory type, study area, current system, number of staff and the support you need.
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