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An independent lab can't fake its way through a regulatory inspection. We list the GLP consultants, QA auditors, and mock-inspection specialists that actually exist — every website load-verified — and match you with quotes from the ones that fit.
Facility, study, data, or report audits before the regulator shows up.
Sourced cost figures and an estimator with visible formulas.
Ten questions, weighted scoring, honest answer in two minutes.
One brief, competing scoped quotes from firms that fit.
GxP compliance consulting firm · Not disclosed
JAF Consulting is a life-science compliance consultancy whose GLP services include laboratory audits, gap analyses, mock FDA inspections, and QMS/SOP support. Its public materials describe hands-on help for ana…
Pharmaceutical GLP consulting firm · Germany
Horn Pharmaceutical Consulting is a Germany-based firm specializing in GLP quality assurance systems. Its public materials describe support for building and running GLP QA functions, auditing nonclinical studie…
GxP consulting firm · Australia
SeerPharma is an Australia-based GxP consultancy offering GLP and GCLP auditing services. Its public materials describe facility, process, study-data, and report auditing against OECD GLP requirements for labor…
Regulatory consulting and talent firm · Not disclosed
The FDA Group provides GLP auditing, mock FDA inspections, gap analysis, and facility qualification alongside SOP development and remediation support. Its published brochure describes GLP laboratory audits and …
Pharmaceutical consulting and services firm · Not disclosed
SciencePharma describes GLP quality-system and nonclinical auditing services, including auditing of bioanalytical studies. Its public materials present GLP support as part of a broader nonclinical and pharmaceu…
Independent GLP consulting practice · Not disclosed
Robin Guy Consulting is an independent practice offering GLP consulting and quality-assurance services, including QA-unit support, SOP work, mock inspections, and training. The practice is led by a registered R…
See all 13 verified GLP providers →
Good Laboratory Practice is the quality system for nonclinical safety studies — the toxicology, pharmacology, and environmental studies that support regulatory submissions. It covers who can run a study (trained personnel, an independent QA unit), where (qualified facilities and equipment), how (approved protocols and SOPs), and what the records look like (complete, attributable, attributable data — ALCOA+). The FDA's GLP regulation is 21 CFR Part 58; internationally, OECD GLP principles govern mutual acceptance of data.
A hard truth this site is built on: no private company can certify you GLP-compliant. GLP recognition comes from national GLP monitoring authorities that inspect facilities. Consultants get you ready and audit you; the regulator decides.
Good Laboratory Practice (GLP) is the quality system governing nonclinical safety studies whose results support regulatory submissions — pharma, biotech, agrochemicals, and industrial chemicals. If your lab generates data for FDA, EPA, or OECD member authorities, the study must run under GLP. GLP covers study management, QA, facilities, equipment, test articles, SOPs, and data integrity.
No — and treat any firm selling one as a red flag. GLP compliance is recognized by national GLP monitoring authorities (e.g. the FDA, or OECD MAD member authorities), which inspect facilities. Consultants and auditors can get your lab GLP-ready and audit it, but they cannot grant GLP status.
Independent GLP audits (facility, study, data, report), gap analyses, mock regulatory inspections, QA-unit support, SOP development, staff training, and remediation help. Many labs hire consultants for a pre-inspection audit so a real inspection has no surprises.
Consultants rarely publish fees. Published GxP audit benchmarks put day rates around $2,250–$4,000/day (see our cost guide for sourced figures). A full GLP program build is a six-figure, multi-year investment — one documented case totaled $623,000 over 3 years.
If you only need occasional regulated studies, a GLP-compliant contract lab (CRO) is usually cheaper and faster. If you run studies continuously, or want control over your data and facility, building an in-house GLP program with consultant support pays off. Our consultant-vs-CRO comparison walks through the math.
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How it works: tell us once (4 questions, 2 min) → we match licensed auditors to your size and scope → they send scoped quotes directly. Free, no obligation.