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Croda Pharma
Open to RFQsSmart science to improve lives
About
Croda Pharma is the pharmaceutical business of Croda International Plc (established 1925, registered office Cowick Hall, Snaith, Goole, East Yorkshire), and describes itself as "a world leader in pharmaceutical excipients, vaccine adjuvants and lipid delivery systems for human and veterinary applications". It combines Croda's speciality excipient portfolio with the lipid delivery systems of Avanti Polar Lipids and an adjuvant systems arm. It states 80+ years of expertise in adjuvant research, that it has been customising lipids since 1950, that it was the first supplier of lipids for a COVID-19 mRNA vaccine, and that its adjuvants feature in 15 of 24 WHO-listed vaccines.
Strategic positioning
Excipients, vaccine adjuvants and lipid delivery systems with in-house formulation support.
Supplier scorecard · deterministic, 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.
Compliance iCounts agency registrations (FDA, EU GMP, MHRA, PMDA, WHO GMP, NMPA, PIC/S) at 6 points each capped at 35, ISO certifications at 5 each capped at 20, GMP status (cGMP commercial 25, GMP 18, Pharma-grade 10), plus DMF 7, CEP 7 and TSE/BSE statement 6. Levels: 80+ Fully GMP-compliant | 60-79 GMP-compliant | 40-59 Developing compliance | below 40 Research-grade. Whether this dimension matters for you depends on your specific project.
25Research-grade
Quality iBlends the reported audit score (up to 40 points), CAPA closure rate (up to 25) and deviation history (starts at 20 and loses 2 points per deviation), plus 8 for CoA availability and 7 for validation packages. Levels: 85+ Excellent quality | 65-84 Strong quality | 45-64 Good quality | below 45 Developing. Whether this dimension matters for you depends on your specific project.
—Not disclosed
Delivery iBlends on-time delivery percentage (up to 50 points), lead time (up to 30 - shorter is better, 2 points lost per week; 15 if not reported) and service level (Emergency supply 20, Expedited 14, Standard 8). Levels: 85+ Highly reliable | 65-84 Reliable | 45-64 Standard | below 45 Variable. Whether this dimension matters for you depends on your specific project.
—Not disclosed
Documentation iCounts documents in the profile vault at 5 points each, capped at 35, plus flags for a Certificate of Analysis (15), validation packages (15), DMF (10), CEP (10) and a TSE/BSE statement (5). Levels: 80+ Full documentation | 60-79 Strong documentation | 40-59 Established | below 40 Basic. Whether this dimension matters for you depends on your specific project.
0Basic
Regulatory iCounts supported regulatory regions at 5 points each capped at 30, the share of on-platform audits with a clean outcome (no action, NAI or pass) worth up to 30 (15 if no audits yet), FDA inspection history (20 if inspected, 10 if only registered) and QMS maturity (Validated 20, Established 12, Basic 4). Levels: 80+ Inspection-proven | 60-79 Strong regulatory | 40-59 Established | below 40 Developing. Whether this dimension matters for you depends on your specific project.
15Developing
Breadth iCounts product categories at 7 points each capped at 35, catalog size at 3 points per listed product capped at 30, modalities served at 4 each capped at 20, plus 8 for sterile-grade and 7 for GMP-grade offerings. Levels: 80+ Broad portfolio | 60-79 Multi-category | 40-59 Focused | below 40 Specialist. Whether this dimension matters for you depends on your specific project.
44Focused
Product categories
ExcipientsVaccine adjuvantsLipid delivery systems
Modalities served
Small moleculesBiologicsVaccinesmRNA / LNP
Manufacturing scale
ClinicalCommercial
Live record · illustrative seed data · scores deterministic, rules-based — not AI.