Sangon Biotech: difference between revisions
Diff·revision 21 → 22·15:18, 22 Nov 2025
Difference between revision 21 and revision 22 of Sangon Biotech. 7 lines changed; the page grew by 1,120 bytes.
| Revision 21 — 05:13, 1 Nov 2025 CrudePeptidePearl (talk) add the see-also to the certificate-of-analysis article 13,424 bytes ±0 | Revision 22 — 15:18, 22 Nov 2025 DataTableDunja (talk) add the note that this wiki publishes no score and no league table 14,544 bytes +1,120 | ||
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| 99 | What is '''not''' available is independent coverage in a source unconnected with the organisation or its customers. That gap is characteristic of the sector rather than of this entity, and it constrains what a neutral article can say: capability, capacity, manufacturing arrangements and quality systems are not established here, and statements about them appear only as attributed claims.{{r|selfpub}} | 99 | What is '''not''' available is independent coverage in a source unconnected with the organisation or its customers. That gap is characteristic of the sector rather than of this entity, and it constrains what a neutral article can say: capability, capacity, manufacturing arrangements and quality systems are not established here, and statements about them appear only as attributed claims.{{r|selfpub}} |
| 100 | 100 | ||
| + | 101 | Two frameworks are named in this article only to say what has ''not'' been established against them: a quality-system claim is not a fact until assessed against the applicable good-manufacturing-practice framework,{{r|gmp}} and a testing laboratory's competence is a matter of accreditation to a recognised standard rather than of self-description.{{r|iso17025}} Neither assessment is available here for this organisation or for any other covered on this wiki. | |
| + | 102 | ||
| + | 103 | == External links == | |
| + | 104 | * [https://sangonbio.com/ Sangon Biotech (Shanghai) Co., Ltd. — official site (sangonbio.com)] — the organisation's own catalogue, stock listing and ordering pages. Marked <code>nofollow</code> and <code>sponsored</code>; PeptidePedia takes no commission and the link is not an endorsement. | |
| + | 105 | * [[Project:Vendor notability]] — why this article carries an outbound link and the organisations listed at the foot of [[Category:Peptide suppliers]] do not. | |
| + | 106 | ||
| 101 | == References == | 107 | == References == |
| 102 | {{reflist}} | 108 | {{reflist}} |
| ⋮ | ⋮ | ||
| 106 | <ref name="tally">PeptidePedia reception tally (self-reported submissions; '''weak evidence''' — see [[Project:Sourcing guidelines]]). Self-selected sample; period and count stated at each point of use.</ref> | 112 | <ref name="tally">PeptidePedia reception tally (self-reported submissions; '''weak evidence''' — see [[Project:Sourcing guidelines]]). Self-selected sample; period and count stated at each point of use.</ref> |
| 107 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, "Quality Attributes of Synthetic Peptide Drug Substances" (informational). USP–NF, current revision.</ref> | 113 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, "Quality Attributes of Synthetic Peptide Drug Substances" (informational). USP–NF, current revision.</ref> |
| + | 114 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories''. International Organization for Standardization.</ref> | |
| 108 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> | 115 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> |
| 109 | <ref name="gmp">World Health Organization, ''Good Manufacturing Practices for Pharmaceutical Products: Main Principles'', WHO Technical Report Series. The general framework against which a GMP claim is assessed.</ref> | 116 | <ref name="gmp">World Health Organization, ''Good Manufacturing Practices for Pharmaceutical Products: Main Principles'', WHO Technical Report Series. The general framework against which a GMP claim is assessed.</ref> |