Verifarma International, S.L. is a life-sciences compliance software company headquartered in Las Palmas de Gran Canaria, Spain, which states it started in 2007 at IAE Business School. Its products are Verifarma Track & Trace (unit-level drug serialisation and aggregation across packaging levels for regulatory traceability), an eQMS covering deviations, audits, complaints and quality programmes, an AI assistant called Vera embedded in the quality solutions, and SAP Business One implementation (offered in Argentina). The company states its platform connects more than 2,000 companies — laboratories, distributors, pharmacies, hospitals and health authorities — across 27 countries.
Deterministic scores · rules-based, not AIiHow these scores are obtained: each one is computed from this profile's listed attributes — capability checkboxes, certifications, capacity figures and coverage — by a fixed formula, recomputed on every page load. Deterministic and rules-based means the score comes from a fixed, transparent formula over listed attributes — the same inputs always produce the same score. It is not AI: there is no model, no learning, and no hidden weighting. Whether a score is relevant to you depends on your specific project: a capability that raises the number may not matter for your work, and a niche strength your project needs may barely move it. Capability scores are a directional starting point, not a verdict. A lower score does not disqualify a company or consultant, and no decision should rest on the score alone — always contact the company directly to confirm the specifics for your project.
GMP expertise iAverages per-area depth across the consultant's listed GMP expertise areas - each area blends proficiency (Foundational 35 up to SME 100, 45%), years of experience (capped at 20, 25%), projects completed (capped at 40, 20%) and inspection support (10%) - then combines 78% depth with 22% breadth (14 points per area, ~7 areas = full breadth). Shows 0 - Developing with no areas listed. Levels: 85+ Elite | 70-84 Advanced | 50-69 Established | below 50 Developing. Whether this dimension matters for you depends on your specific project.
0Developing
Functional depth iAverages each functional specialization group - 60% its SME level (Practitioner 45 up to Authority 100) plus 40% its skill count (20 points per skill, capped) - then combines 75% depth with 25% breadth (17 points per group, ~6 groups = full breadth). Shows 0 - Developing with no groups listed. Levels: 85+ Authority | 70-84 Advanced | 50-69 Established | below 50 Developing. Whether this dimension matters for you depends on your specific project.
0Developing
Regulatory iAdds inspections supported (4 points each, capped at 40), remediations led including Warning-Letter and data-integrity work (5 points each, capped at 30) and regulatory agencies covered (5 points each, capped at 20), plus a 10-point credit for any Warning-Letter remediation. Levels: 80+ Authority | 60-79 Seasoned | 40-59 Experienced | below 40 Emerging. Whether this dimension matters for you depends on your specific project.
20Emerging
Engagement iHow fast and flexibly the consultant can start: availability status (Available now 35, Limited 22, otherwise 10), typical response time (same-day/24h 25, 48h 15, any stated time 8), engagement models offered (6 points each, capped at 25), plus 8 for remote availability and 7 for willingness to travel. Levels: 80+ Immediate | 60-79 Ready | 40-59 Available | below 40 Limited. Whether this dimension matters for you depends on your specific project.
10Limited
Audit readiness iCounts agencies with at least one supported inspection (FDA, EMA, MHRA, PMDA, Health Canada, WHO - 5 points each, capped at 25), total inspections and audits (1.2 points each, capped at 30), mock inspections (3 each, capped at 10), the reported inspection success rate (up to 20; assumed 70% if unreported) and remediations (2.5 each, capped at 15). Levels: 85+ Inspection-ready | 70-84 Strong | 50-69 Established | below 50 Developing. Whether this dimension matters for you depends on your specific project.
14Developing
Industry maturity iClinical-to-commercial lifecycle reach: commercial launches (6 points each, capped at 24), facility startups (3 each, capped at 18), greenfield plus brownfield projects (2.5 each, capped at 14), facilities supported (0.7 each, capped at 14) and manufacturing scales covered (3 each, capped at 12, plus 8 if commercial scale), plus 2 points per industry served, capped at 10. Levels: 85+ Commercial-grade | 70-84 Advanced | 50-69 Established | below 50 Emerging. Whether this dimension matters for you depends on your specific project.
0Emerging
Regulatory agencies
Verifarma publishes the following claims on its own site: "ISO 9001 — Quality Management""ISO 27001 — Information Security""Validated in accordance with GAMP 5""GS1 — Meeting standards since 2008""FDA 21 CFR Part 11 — FDA compliance and digital signatures""EU ANNEX 11 — Compliance with EU guidelines"and GMP. It is also a Certified B Corporation ("Empresa B Certificada"). Traceability regimes named for its Track & Trace product include EU FMDANMAT (Argentina) and INVIMA (Colombia). Only iso9001 was flagged: the 21 CFR Part 11 and Annex 11 statements are software-compliance claimsnot an FDA establishment registration or an EU GMP authorisationand must not be encoded as such.
Primary specializations
Track and Trace (pharmaceutical serialisation and traceability)eQMS
Coverage regions
Headquarters at 8 Churruca StreetLas Palmas de Gran CanariaSpainwith offices in Argentina (Vicente LópezBuenos Aires)Mexico and Ecuador. Verifarma states operations in 27 countriesnaming among them the EUArgentinaUSACanadaChinaIndiaRussiaSaudi ArabiaTurkeySouth KoreaKazakhstanUAE and Uzbekistan.
VI
Verifarma International
We promote pharmaceutical traceability at a global level.