VaccineEmulsionStability_QualityChecker

Vaccine Emulsion Stability

Vet veterinary veterinary vaccines animal health adjuvants aquaculture batch release CSV→JSON
Open selection

Utility description: Vaccine Emulsion Stability

Vaccine Emulsion Stability Quality Checker — Control of Vaccine Emulsion Stability

ℹ️  Utility assesses the quality of adjuvant emulsions (mainly Water-in-Oil W/O) for veterinary vaccines according to Ph. Eur. 5.2.3 and manufacturer standards (HIPRA, Biogénesis Bagó):
     • Droplet Size: Mean diameter and D90 (diameter below which 90% of droplets fall). Large droplets cause local reactions.
     • Viscosity: Determines the ability of the emulsion to pass through a syringe needle (Injectability).
     • Stability Index: Percentage of phase separation after centrifugation or storage.
     • Emulsion Type: Confirmation of type (W/O or O/W) by measuring conductivity.

⚠️  CRITICAL: Presence of droplets larger than 5-6 µm (D90 > 5-6) sharply increases the risk of sterile abscesses and granulomas at the injection site!
     Emulsion breaking leads to the animal receiving either pure oil or aqueous phase without adjuvant.

Usage:
  VaccineEmulsionStabilityQualityChecker.exe                            → demo mode (console output)
  VaccineEmulsionStabilityQualityChecker.exe input.csv output.json      → evaluate your data

Input format:
BatchNumber,ProductName,DropletSize_Mean_um,DropletSize_D90_um,Viscosity_cP,StabilityIndex_Percent,PhaseInversionTemp_C,EmulsionType,Conductivity_uS_cm

Example:
  EMUL-2026-FMD-001,FMD Vaccine,1.2,3.5,450.0,5.0,65.0,W/O,2.0

— WHY IS THIS NEEDED?
Oil-based adjuvants (e.g., Montanide, Marcol) are used to create an antigen depot and enhance immune response.
Emulsification quality directly affects reactogenicity (safety) and immunogenicity (efficacy) of the vaccine.
A stable emulsion ensures slow release of the antigen.

⚠️  CRITICAL:
• Droplet Size: Should be as small as possible (ideally < 2 µm) to reduce viscosity and reactogenicity.
• Viscosity: Too high viscosity makes administration by veterinarian or farmer difficult.
• Stability: Emulsion must withstand temperature fluctuations during transport without separation.
• Emulsion Type: W/O (Water-in-Oil) has low conductivity as the external phase is oil (dielectric). Error in emulsion type is critical for mechanism of action.

Key features:
• Control of granulometric composition (droplet size)
• Assessment of rheological properties (viscosity)
• Physical stability check (separation)
• Emulsion type verification by conductivity
• Generation of reports for R&D and QC departments, and LIMS LabWare
• Compliance with Ph. Eur. 5.2.3 and GMP requirements

Critical parameters:
• Mean Droplet Size: ≤ 2.5 µm
• D90 Droplet Size: ≤ 5.0 µm
• Viscosity: 200–800 cP (depends on oil type)
• Stability Index: ≤ 10%
• Conductivity (for W/O): < 20 µS/cm

💡 Usage tips:
1. Size Measurement Method: Use laser diffraction or microscopy with image analysis.
2. Temperature: Measure viscosity at application temperature (usually 20-25°C), as cold oil is very viscous.
3. Stability Test: Standard test includes centrifugation at 3000-4000 rpm for 30 minutes.
4. Homogenization: Production process must ensure high homogenization pressure to achieve fine dispersity.
5. Storage: Avoid freezing W/O emulsions, as ice crystals destroy the emulsion structure.

⚠️ Note: Veterinary medicine often uses more viscous and "coarser" emulsions than human medicine due to differences in reactogenicity requirements for different animal species (cattle, pigs, poultry).

input.csv

BatchNumber,ProductName,DropletSize_Mean_um,DropletSize_D90_um,Viscosity_cP,StabilityIndex_Percent,PhaseInversionTemp_C,EmulsionType,Conductivity_uS_cm
EMUL-2026-FMD-001,FMD Vaccine (W/O),1.2,3.5,450.0,5.0,65.0,W/O,2.0
EMUL-2026-NDV-002,Newcastle Disease Vaccine (O/W),0.5,1.2,15.0,2.0,N/A,O/W,1200.0
EMUL-2026-FAIL-003,Rabies Vaccine (W/O),4.5,8.2,900.0,15.0,60.0,W/O,5.0

URS & FS — User Requirements and Functional Specification

This document describes the controlled interface and behaviour of VaccineEmulsionStability_QualityChecker for Vaccine Emulsion Stability Quality Checker.

Domain limits and critical parameters

Key fragments from the source description are shown below. Before production use, limits must be verified against the approved specification, registration dossier and local SOPs.
  • ℹ️ Utility assesses the quality of adjuvant emulsions (mainly Water-in-Oil W/O) for veterinary vaccines according to Ph. Eur. 5.2.3 and manufacturer standards (HIPRA, Biogénesis Bagó):
  • • Droplet Size: Mean diameter and D90 (diameter below which 90% of droplets fall). Large droplets cause local reactions.
  • ⚠️ CRITICAL: Presence of droplets larger than 5-6 µm (D90 > 5-6) sharply increases the risk of sterile abscesses and granulomas at the injection site!
  • ⚠️ CRITICAL:
  • • Droplet Size: Should be as small as possible (ideally < 2 µm) to reduce viscosity and reactogenicity.
  • • Stability: Emulsion must withstand temperature fluctuations during transport without separation.
  • • Emulsion Type: W/O (Water-in-Oil) has low conductivity as the external phase is oil (dielectric). Error in emulsion type is critical for mechanism of action.
  • • Compliance with Ph. Eur. 5.2.3 and GMP requirements
  • Critical parameters:
  • • Mean Droplet Size: ≤ 2.5 µm
  • • D90 Droplet Size: ≤ 5.0 µm
  • • Stability Index: ≤ 10%
  • • Conductivity (for W/O): < 20 µS/cm
  • 4. Homogenization: Production process must ensure high homogenization pressure to achieve fine dispersity.

URS — User Requirements Specification

IDRequirementCriticalityAcceptance criterion
URS-001The utility shall accept an input.csv file for Vaccine Emulsion Stability Quality Checker with headers defined in the data contract.HighThe file is processed without manual header editing.
URS-002The utility shall perform deterministic QC evaluation without machine learning and without probabilistic conformance decisions.HighIdentical input data, rule version and configuration produce reproducible results.
URS-003The utility shall validate mandatory fields, data types, ranges, units and domain plausibility.HighSchema, conversion and range errors are explicitly reported.
URS-004The utility shall apply domain limits and rules from the description, approved specification, registration dossier and local SOPs.HighEach check has PASS/WARNING/FAIL and a clear message.
URS-005The utility shall generate output.json with machine-readable results, source values, warnings, failures and critical findings.HighJSON is suitable for LIMS/ELN/MES integration and QA/QC review.
URS-006The utility shall preserve traceability between batch/sample, input file, applied rules and final status.HighOutput contains identifiers, checked parameters and audit metadata.
URS-007The documentation shall support IQ/OQ/PQ, CSV/CSA and review by internal QA or inspectors.MediumURS, FS, input/output contract and test scenarios are supplied with the utility.
URS-008The utility shall be used as a QC decision-support tool and not as a substitute for approved specifications and QA/QP release decision.MediumDocumentation states change control and limit-verification expectations.

input.csv contract

#FieldTypeSamplePurpose
1BatchNumberstring / controlled vocabularyEMUL-2026-FMD-001Batch or lot identifier used for traceability.
2ProductNamestring / controlled vocabularyFMD Vaccine (W/O)Product or dosage-form name under evaluation.
3DropletSize_Mean_umdecimal1.2Controlled input parameter for deterministic QC rules.
4DropletSize_D90_umdecimal3.5Controlled input parameter for deterministic QC rules.
5Viscosity_cPdecimal450.0Controlled input parameter for deterministic QC rules.
6StabilityIndex_Percentdecimal5.0Controlled input parameter for deterministic QC rules.
7PhaseInversionTemp_Cstring / controlled vocabulary65.0pH; parameter relevant to stability, compatibility and batch suitability.
8EmulsionTypestring / controlled vocabularyW/OControlled input parameter for deterministic QC rules.
9Conductivity_uS_cmdecimal2.0Controlled input parameter for deterministic QC rules.
BatchNumber,ProductName,DropletSize_Mean_um,DropletSize_D90_um,Viscosity_cP,StabilityIndex_Percent,PhaseInversionTemp_C,EmulsionType,Conductivity_uS_cm
EMUL-2026-FMD-001,FMD Vaccine (W/O),1.2,3.5,450.0,5.0,65.0,W/O,2.0
EMUL-2026-NDV-002,Newcastle Disease Vaccine (O/W),0.5,1.2,15.0,2.0,N/A,O/W,1200.0
EMUL-2026-FAIL-003,Rabies Vaccine (W/O),4.5,8.2,900.0,15.0,60.0,W/O,5.0

Input validation rules

IDFieldRuleCriticality
VR-001BatchNumberThe field shall match an approved dictionary or accepted string representation.High
VR-002ProductNameThe field shall match an approved dictionary or accepted string representation.High
VR-003DropletSize_Mean_umThe field shall match an approved dictionary or accepted string representation.High
VR-004DropletSize_D90_umThe field shall match an approved dictionary or accepted string representation.Medium
VR-005Viscosity_cPThe field shall match an approved dictionary or accepted string representation.Medium
VR-006StabilityIndex_PercentThe field shall match an approved dictionary or accepted string representation.Medium
VR-007PhaseInversionTemp_CThe field shall match an approved dictionary or accepted string representation.Medium
VR-008EmulsionTypeThe field shall match an approved dictionary or accepted string representation.Medium
VR-009Conductivity_uS_cmThe field shall match an approved dictionary or accepted string representation.Medium

FS — Functional Specification

IDFunctionImplementation
FS-001CLI executionSupport execution modes: demo mode without arguments and production mode input.csv output.json.
FS-002CSV importRead input.csv in UTF-8/CSV-compatible format and validate header and expected columns.
FS-003Schema validationCheck mandatory fields, column count, unknown key fields and empty mandatory values.
FS-004Type conversionConvert numeric, flag and text values; invalid format is recorded as a row-level error.
FS-005Domain rule engineApply rules for Vaccine Emulsion Stability Quality Checker, including critical limits from the description and approved specification.
FS-006Status aggregationProduce final status: FAIL for critical failure, WARNING for non-critical deviation, PASS for conformance.
FS-007JSON exportWrite output.json with detailed checks, source values, warnings, failures and critical findings.
FS-008Audit supportKeep result structure suitable for review, deviation investigation and calculation reproduction.
FS-009Integration contractSupport the scenario LIMS/ELN/MES → input.csv → utility → output.json → portal/admin review.
FS-010Error handlingReturn explicit messages for missing file, empty CSV, invalid schema, output write failure and invalid format.

Example output.json

{
  "utilityId": "vaccineemulsionstability-qualitychecker",
  "utilityFolder": "VaccineEmulsionStability_QualityChecker",
  "package": "Vet",
  "overallStatus": "PASS|WARNING|FAIL",
  "sourceFile": "input.csv",
  "processedAtUtc": "2026-06-10T00:00:00Z",
  "checks": [
    {
      "parameter": "BatchNumber",
      "value": "EMUL-2026-FMD-001",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-001"
    },
    {
      "parameter": "ProductName",
      "value": "FMD Vaccine (W/O)",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-002"
    },
    {
      "parameter": "DropletSize_Mean_um",
      "value": "1.2",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-003"
    },
    {
      "parameter": "DropletSize_D90_um",
      "value": "3.5",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-004"
    },
    {
      "parameter": "Viscosity_cP",
      "value": "450.0",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-005"
    },
    {
      "parameter": "StabilityIndex_Percent",
      "value": "5.0",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-006"
    },
    {
      "parameter": "PhaseInversionTemp_C",
      "value": "65.0",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-007"
    },
    {
      "parameter": "EmulsionType",
      "value": "W/O",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-008"
    },
    {
      "parameter": "Conductivity_uS_cm",
      "value": "2.0",
      "status": "PASS|WARNING|FAIL",
      "message": "Deterministic rule-based check result",
      "ruleReference": "FS-RULE-009"
    }
  ],
  "criticalFindings": [],
  "warnings": [],
  "audit": {
    "inputHash": "sha256:<calculated at runtime>",
    "rulesVersion": "<utility executable version>",
    "documentation": "VaccineEmulsionStability_QualityChecker.documentation.html"
  }
}

Traceability matrix

URSFSTestEvidence
URS-001FS-001, FS-002OQ-001Verify execution and import of valid input.csv.
URS-002FS-005, FS-006OQ-004Repeat the same dataset and compare output.json.
URS-003FS-003, FS-004, FS-010OQ-002, OQ-003Verify missing columns and invalid types.
URS-004FS-005, FS-006OQ-004, PQ-001Verify critical deviations on real/boundary data.
URS-005FS-007, FS-009OQ-005Verify JSON schema and downstream-system suitability.
URS-006FS-008OQ-006Verify identifiers and audit metadata.
URS-007FS-008, FS-010IQ-001, OQ-007Verify documentation completeness and control evidence.
URS-008FS-005, FS-008PQ-002Verify review workflow and no replacement of QA decision.

IQ/OQ/PQ test scenarios

IDScenarioExpected result
IQ-001Verify executable, input.csv, documentation and checksum availability.Delivery set is complete; version is recorded.
OQ-001Valid sample row from input.csv.PASS or acceptable WARNING according to rules.
OQ-002Remove a mandatory CSV column.Schema error or FAIL with missing-column reference.
OQ-003Place a non-numeric value into a numeric field.Type-conversion error with row/field reference.
OQ-004Set a critical parameter outside the limit.FAIL and critical finding.
OQ-005Verify output.json structure.All mandatory sections are present and JSON is valid.
OQ-006Verify batch/sample traceability.Input and result identifiers match.
PQ-001Verify 3–5 real user batches/samples.Result is confirmed by QC/QA review.
PQ-002Verify deviation workflow and manual QA decision.Utility supports review but does not replace approved decision.

QA/QC and change control

  • Do not rename columns without updating validator, documentation and test set.
  • Retain input.csv, output.json, executable version and checksum.
  • Before production use, perform IQ/OQ/PQ or equivalent CSV/CSA verification.
  • Critical limits shall be verified against the approved specification, registration dossier and local SOPs.
  • The utility provides structured QC decision support; final release decision remains with QA/QP and approved procedures.

Included in packages

Vet — Veterinary QC Utilities

Vet is designed for veterinary pharmaceuticals and vaccines: adjuvants, antigens, autogenous vaccines, aquaculture, feed/premixes, antimicrobial and antiparasitic products, sterility and batch release.

Open