SitagliptinMetforminQualityChecker

Sitagliptin Metformin

API assay biologics biosimilars dissolution fixed-dose combinations generics heavy metals
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Sitagliptin Metformin Quality Checker — Combo Product (Diabetes)

ℹ️ The utility checks content of both APIs, NDMA (nitrosamines) in metformin, sitagliptin uniformity.
ℹ️ Does not use machine learning — rule-based logic only.
⚠️ CRITICAL! NDMA ≤96 ppb. Uniformity RSD ≤6.0%. Dissolution ≥80% in 30 min!

Usage:
SitagliptinMetforminQualityChecker.exe → demo mode
SitagliptinMetforminQualityChecker.exe input.csv output.json → evaluate data

Input format:
BatchNumber,Sitagliptin_Content_Percent,Metformin_Content_Percent,Sita_Impurity_A_Percent,Sita_Total_Impurities_Percent,Metformin_NDMA_ppb,Metformin_Total_Impurities_Percent,Total_All_Impurities_Percent,Loss_On_Drying_Percent,Heavy_Metals_ppm,Dissolution_Sita_30min_Percent,Dissolution_Met_30min_Percent,Content_Uniformity_RSD,Microbial_Count_TAMC,Microbial_Count_TYMC,EColi_Detected,Salmonella_Detected

Example:
SITA-MET-2026-001,98.8,99.2,0.05,0.2,30.0,0.3,0.5,0.4,6,92.0,94.0,3.5,30,8,0,0

— WHY IS THIS NEEDED?
Sitagliptin + Metformin combination used for type 2 diabetes treatment:
• Metformin is prone to nitrosamine (NDMA) formation, which are carcinogens. NDMA control is critical and strictly regulated (limit usually <96 ppb).
• Sitagliptin has a low dose compared to metformin, so Content Uniformity (CU) is strictly controlled.
• Synchronous release of both components important for comprehensive therapeutic effect (glucose lowering by different mechanisms).
• Drug taken long-term, so heavy metal and microbiology control important.
⚠️ CRITICAL:
• Content of both APIs: 95–105%
• NDMA (in metformin): ≤ 96 ppb (strict regulatory limit)
• Uniformity (RSD): ≤ 6.0%
• Dissolution: ≥ 80% in 30 min for both components
• Heavy Metals: ≤ 10 ppm
• Microbiology: absence of pathogens
⚠️ Note: Utility focuses on metformin safety (nitrosamines) and sitagliptin quality (uniformity). Exceeding NDMA level is ground for immediate batch rejection due to patient health risk. Dissolution synchronicity ensures simultaneous action of DPP-4 inhibitor and insulin sensitizer.

input.csv

BatchNumber,Sitagliptin_Content_Percent,Metformin_Content_Percent,Sita_Impurity_A_Percent,Sita_Total_Impurities_Percent,Metformin_NDMA_ppb,Metformin_Total_Impurities_Percent,Total_All_Impurities_Percent,Loss_On_Drying_Percent,Heavy_Metals_ppm,Dissolution_Sita_30min_Percent,Dissolution_Met_30min_Percent,Content_Uniformity_RSD,Microbial_Count_TAMC,Microbial_Count_TYMC,EColi_Detected,Salmonella_Detected
SITA-MET-2026-001,98.8,99.2,0.05,0.2,30.0,0.3,0.5,0.4,6,92.0,94.0,3.5,30,8,0,0

URS & FS — user requirements and functional specification

This document defines user requirements and functional specification for the quality-control utility. It supports deployment discussion, IQ/OQ preparation and QC workflow integration.

Utility: SitagliptinMetforminQualityCheckerAPI / object: Sitagliptin MetforminCategory: Global API

1. Scope

The Sitagliptin Metformin Quality Checker utility is used for Sitagliptin Metformin. The actual input.csv is the source of truth for the input structure; control criteria are defined by the executable and the domain description.

The utility does not use machine learning; decisions are produced by deterministic rules.

Categories: Global API

Tags: API, assay, biologics, biosimilars, dissolution, fixed-dose combinations, generics, heavy metals, impurities, market map, microbiology, uniformity

2. Execution modes

SitagliptinMetforminQualityChecker.exe                            → demo mode
SitagliptinMetforminQualityChecker.exe input.csv output.json      → evaluate data

3. Key controlled areas

  • assay / content
  • purity and impurities
  • dissolution / disintegration
  • microbiology and pathogens
  • heavy metals / elemental impurities

4. Domain limits and critical parameters

  • ⚠️ CRITICAL! NDMA ≤96 ppb. Uniformity RSD ≤6.0%. Dissolution ≥80% in 30 min!
  • Metformin is prone to nitrosamine (NDMA) formation, which are carcinogens. NDMA control is critical and strictly regulated (limit usually <96 ppb).
  • ⚠️ CRITICAL:
  • Content of both APIs: 95–105%
  • NDMA (in metformin): ≤ 96 ppb (strict regulatory limit)
  • Uniformity (RSD): ≤ 6.0%
  • Dissolution: ≥ 80% in 30 min for both components
  • Heavy Metals: ≤ 10 ppm
  • Microbiology: absence of pathogens
  • ⚠️ Note: Utility focuses on metformin safety (nitrosamines) and sitagliptin quality (uniformity). Exceeding NDMA level is ground for immediate batch rejection due to patient health risk. Dissolution synchronicity ensures simultaneous action of DPP-4 inhibitor and insulin sensitizer.
Limits stated in the description must be verified against the current approved specification, pharmacopoeial monograph and registration dossier before production use.

5. URS — user requirements

IDRequirementCriticalityAcceptance criterion
URS-001The system shall accept an input.csv file for Sitagliptin Metformin with the exact columns listed in the “Input data contract” section.HighA file with the correct header is processed without manual editing; missing mandatory columns produce FAIL/import error.
URS-002The system shall support execution without arguments in demo mode and execution with input.csv output.json for user data.MediumBoth execution scenarios produce a predictable result or clear diagnostic error.
URS-003The system shall perform rule-based controls for: assay / content, purity and impurities, dissolution / disintegration, microbiology and pathogens, heavy metals / elemental impurities.HighEach controlled parameter receives a status and message; the result does not depend on hidden Excel formulas or ML.
URS-004The system shall preserve traceability between batch/lot, source values, applied rules and final verdict.HighOutput includes batch identifier, source values, parameter statuses and critical findings.
URS-005The system shall generate machine-readable output.json for LIMS/ELN/MES, batch record and QA/QC review.HighJSON contains overall status, check array, warnings, failures and source-file reference.
URS-006The system shall support use in the client validation package: URS/FS, IQ/OQ preparation, installation and operational scenario checks.HighThe document, test scenarios and reproducible CSV/JSON flow are suitable for audit and internal approval.
URS-007The system shall clearly separate technical data errors from specification nonconformities.MediumSchema/type errors are not mixed with pharmacopoeial deviations and are reported separately.

6. input.csv data contract

The source of truth for the input schema is the actual input.csv header. Column names are technical identifiers and are not translated.

#ColumnTypeUnitDescriptionSampleControl rule
1BatchNumberidentifieras specifiedBatch NumberSITA-MET-2026-001mandatory field; used for batch/lot traceability
2Sitagliptin_Content_Percentdecimal%Sitagliptin Content %98.8numeric value; compared with assay/purity limit from specification or method
3Metformin_Content_Percentdecimal%Metformin Content %99.2numeric value; compared with assay/purity limit from specification or method
4Sita_Impurity_A_Percentdecimal%Sita Impurity A %0.05numeric value; compared with individual or total impurity limit
5Sita_Total_Impurities_Percentdecimal%Sita Total Impurities %0.2mandatory numeric value; rule comparison is performed by the utility
6Metformin_NDMA_ppbdecimalppbMetformin NDMA ppb30.0mandatory numeric value; rule comparison is performed by the utility
7Metformin_Total_Impurities_Percentdecimal%Metformin Total Impurities %0.3mandatory numeric value; rule comparison is performed by the utility
8Total_All_Impurities_Percentdecimal%Total All Impurities %0.5mandatory numeric value; rule comparison is performed by the utility
9Loss_On_Drying_Percentdecimal%Loss On Drying %0.4mandatory numeric value; rule comparison is performed by the utility
10Heavy_Metals_ppmdecimalppmHeavy Metals ppm6numeric value; checked as elemental/metal impurity
11Dissolution_Sita_30min_Percentdecimal%Dissolution Sita 30min %92.0numeric value; dissolution/disintegration profile checked according to method
12Dissolution_Met_30min_Percentdecimal%Dissolution Met 30min %94.0numeric value; dissolution/disintegration profile checked according to method
13Content_Uniformity_RSDdecimalas specifiedContent Uniformity RSD3.5numeric value; compared with assay/purity limit from specification or method
14Microbial_Count_TAMCdecimalas specifiedMicrobial Count TAMC30numeric value; compared with microbiological limits
15Microbial_Count_TYMCdecimalas specifiedMicrobial Count TYMC8numeric value; compared with microbiological limits
16EColi_Detectedboolean / flag0/1EColi Detected0valid flag required; prohibited organisms and growth are normally expected as 0 / absent
17Salmonella_Detectedboolean / flag0/1Salmonella Detected0valid flag required; prohibited organisms and growth are normally expected as 0 / absent

CSV example

BatchNumber,Sitagliptin_Content_Percent,Metformin_Content_Percent,Sita_Impurity_A_Percent,Sita_Total_Impurities_Percent,Metformin_NDMA_ppb,Metformin_Total_Impurities_Percent,Total_All_Impurities_Percent,Loss_On_Drying_Percent,Heavy_Metals_ppm,Dissolution_Sita_30min_Percent,Dissolution_Met_30min_Percent,Content_Uniformity_RSD,Microbial_Count_TAMC,Microbial_Count_TYMC,EColi_Detected,Salmonella_Detected
SITA-MET-2026-001,98.8,99.2,0.05,0.2,30.0,0.3,0.5,0.4,6,92.0,94.0,3.5,30,8,0,0

7. FS — functional specification

IDFunctionImplementation description
FS-001CLI entry pointThe executable SitagliptinMetforminQualityChecker.exe supports demo mode and input.csv output.json processing mode.
FS-002CSV parserThe import module reads CSV, validates header, column presence/order, value count and encoding. Decimal values are expected with a dot separator.
FS-003Field conversionEach column is converted to the expected type: identifier, text, decimal number, date/time or boolean flag.
FS-004Domain rule engineFor Sitagliptin Metformin, explicit rules are applied: range, minimum, maximum, absence of prohibited flag, data completeness or calculation-based check.
FS-005Criticality handlingCritical violations produce FAIL; non-critical deviations and incomplete data produce WARNING; full conformance produces PASS.
FS-006JSON writeroutput.json stores overall status, per-parameter results, source values, warnings, failures and diagnostic messages.
FS-007Integration contractThe CSV → JSON format is stable for invocation from LIMS/ELN/MES, scheduled task or wrapper service.
FS-008Error handlingSchema error, missing file, non-numeric value or JSON write failure returns diagnosable error without silent PASS.

8. output.json contract

The output file must be suitable for automated processing, audit review and correlation with the source input.csv row.

{
  "utility": "SitagliptinMetforminQualityChecker",
  "api": "Sitagliptin Metformin",
  "batchNumber": "SITA-MET-2026-001",
  "overallStatus": "PASS|WARNING|FAIL",
  "checkedAtUtc": "2026-05-18T00:00:00Z",
  "checks": [
    {
      "parameter": "BatchNumber",
      "value": "SITA-MET-2026-001",
      "unit": "as specified",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Sitagliptin_Content_Percent",
      "value": "98.8",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Metformin_Content_Percent",
      "value": "99.2",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Sita_Impurity_A_Percent",
      "value": "0.05",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Sita_Total_Impurities_Percent",
      "value": "0.2",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Metformin_NDMA_ppb",
      "value": "30.0",
      "unit": "ppb",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Metformin_Total_Impurities_Percent",
      "value": "0.3",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    },
    {
      "parameter": "Total_All_Impurities_Percent",
      "value": "0.5",
      "unit": "%",
      "status": "PASS|WARNING|FAIL",
      "message": "Rule-based check result"
    }
  ],
  "criticalFindings": [],
  "sourceFile": "input.csv"
}

9. OQ/PQ test scenarios

IDScenarioExpected result
TC-001Valid CSV with expected header and sample rowAll rows are processed; output contains PASS/WARNING/FAIL and parameter-level detail.
TC-002A mandatory input.csv column is missingImport is rejected or the row receives FAIL with schema reference.
TC-003A numeric field contains text or a blank valueType conversion error is recorded; the result is not hidden as PASS.
TC-004A parameter is outside specification or critical limitCritical parameters produce FAIL; non-critical deviations produce WARNING according to the rule.
TC-005Positive pathogen/microbiological flag or microbiological limit excursionCritical FAIL is produced with the offending parameter.
TC-006Insufficient dissolution or excessive disintegration timeFAIL/WARNING is produced according to method criticality.

10. QA/QC, CSV and change control

  • Before production use, the client records executable version, checksum, specification/monograph version, test CSV, expected JSON and IQ/OQ results.
  • Column names must not be changed without updating the validator and test scenarios.
  • The source CSV, output.json and utility version should be stored together as an evidence package.
  • Any change in control rules must go through change control and repeated OQ scenario verification.

Included in packages

Diabetes QC Suite

QC package for diabetes medicines: insulins, metformin, SGLT2/DPP-4/GLP-1 products, glucagon and supporting dosage-form quality checks.

Open

Endocrinology QC Suite

QC package for endocrinology: thyroid, pituitary/peptide hormones, corticosteroids, sex hormones and selected metabolic medicines.

Open

Global API & Biosimilars QC Suite

Package for high-demand global APIs, generics and biosimilars, including fixed-dose combinations and biological products.

Open