Test report forgery: difference between revisions
Diff·revision 18 → 19·13:53, 24 Jun 2025
Difference between revision 18 and revision 19 of Test report forgery. 7 lines changed; the page grew by 852 bytes.
| Revision 18 — 11:13, 10 Jun 2025 ProglucagonPia (talk) split §What a report shows from §What it does not 4,203 bytes ±0 | Revision 19 — 13:53, 24 Jun 2025 ColumnOvenCoy (talk) clarify that a QR code on a certificate proves issuance, not content 5,055 bytes +852 | ||
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| 39 | The absence of such signals establishes nothing at all. A competent fabrication is internally consistent by construction. | 39 | The absence of such signals establishes nothing at all. A competent fabrication is internally consistent by construction. |
| 40 | 40 | ||
| + | 41 | == Consequences for how documents are used == | |
| + | 42 | This wiki records what documents assert and attributes those assertions to the documents. It does not hold samples, does not verify documents with issuing laboratories, and does not treat a certificate as evidence of the property it reports.{{r|reports}} | |
| + | 43 | ||
| + | 44 | The practical position that follows is not that documents are worthless. A supplier that issues lot-specific certificates naming its methods, retrievable years later against a lot identifier, has built something that is expensive to fake consistently over time — and consistency over time is a stronger signal than any single document. That is a statement about a records system rather than about any one certificate.{{r|iso9001}} | |
| + | 45 | ||
| 41 | == References == | 46 | == References == |
| 42 | {{reflist}} | 47 | {{reflist}} |
| ⋮ | ⋮ | ||
| 44 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref> | 49 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref> |
| 45 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories'', clause 7.8 (reporting of results).</ref> | 50 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories'', clause 7.8 (reporting of results).</ref> |
| + | 51 | <ref name="iso9001">ISO 9001:2015, ''Quality management systems — Requirements''.</ref> | |
| 46 | 52 | ||
| 47 | == See also == | 53 | == See also == |
| ⋮ | ⋮ | ||
| 51 | * [[Lot traceability]] | 57 | * [[Lot traceability]] |
| 52 | * [[VendorInvestigate]] | 58 | * [[VendorInvestigate]] |
| + | 59 | * [[Counterfeit peptide]] | |
| 53 | 60 | ||
| 54 | {{DEFAULTSORT:Test report forgery}} | 61 | {{DEFAULTSORT:Test report forgery}} |