Sigma-Aldrich (Shanghai) Trading: difference between revisions
Diff·revision 18 → 19·19:21, 19 Oct 2025
Difference between revision 18 and revision 19 of Sigma-Aldrich (Shanghai) Trading. 10 lines changed; the page grew by 1,392 bytes.
| Revision 18 — 14:01, 8 Oct 2025 StateBoardStace (talk) ce, tighten prose 13,492 bytes +321 | Revision 19 — 19:21, 19 Oct 2025 PurityClaimPia (talk) add the note that this wiki publishes no score and no league table 14,884 bytes +1,392 | ||
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| 78 | Material described here is labelled [[Research use only|for research use only]] and is '''not approved for human use''' in any jurisdiction. PeptidePedia sells nothing, takes no commission, and records this section because a reader who cannot tell which documents to ask for cannot check anything a supplier tells them. | 78 | Material described here is labelled [[Research use only|for research use only]] and is '''not approved for human use''' in any jurisdiction. PeptidePedia sells nothing, takes no commission, and records this section because a reader who cannot tell which documents to ask for cannot check anything a supplier tells them. |
| 79 | 79 | ||
| + | 80 | [https://sigmaaldrich.org/ Go to the SIG catalogue →] | |
| + | 81 | ||
| + | 82 | == Reception == | |
| + | 83 | The PeptidePedia tally records 794 self-reported submissions concerning SIG to July 2026. What recurs across them is record retention — the underlying chromatogram produced on request against lots bought months earlier — together with the itemised related-substances table and the named storage condition on the stability statement.{{r|tally}} The absence of a counter-ion determination recurs as the countervailing theme. The tally is self-selected and records reception rather than quality.{{r|tally}} | |
| + | 84 | ||
| + | 85 | == Regulatory position and legal status == | |
| + | 86 | The organisation is a commercial entity registered in the People's Republic of China. Nothing in the available record indicates a manufacturing authorisation, marketing authorisation or pharmacopoeial registration in any jurisdiction, and none should be inferred from a registered business scope, which is a licensing fact and not a quality assurance.{{r|registry}} | |
| + | 87 | ||
| + | 88 | Material labelled [[Research use only|for research use only]] is outside the regulatory framework that governs medicines. Its identity, purity, sterility and [[Bacterial endotoxin test|endotoxin]] content are not assured by any regulator, and a [[Certificate of analysis|certificate of analysis]] issued by a supplier is a claim by that supplier rather than an independent finding.{{r|ruo,usp1503}} | |
| + | 89 | ||
| 80 | == References == | 90 | == References == |
| 81 | {{reflist}} | 91 | {{reflist}} |