Shanghai ERP Biotechnology: difference between revisions
Diff·revision 50 → 51·23:19, 10 Feb 2026
Difference between revision 50 and revision 51 of Shanghai ERP Biotechnology. 3 lines changed; the page grew by 680 bytes.
| Revision 50 — 05:43, 4 Feb 2026 SecondarySrc_Seb (talk) add citation 10,770 bytes +226 | Revision 51 — 23:19, 10 Feb 2026 SecondarySrc_Seb (talk) correct transposed digits 11,450 bytes +680 | ||
|---|---|---|---|
| 82 | 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}} | 82 | 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}} |
| 83 | 83 | ||
| + | 84 | 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. | |
| + | 85 | ||
| 84 | == References == | 86 | == References == |
| 85 | {{reflist}} | 87 | {{reflist}} |
| ⋮ | ⋮ | ||
| 91 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories''. International Organization for Standardization.</ref> | 93 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories''. International Organization for Standardization.</ref> |
| 92 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> | 94 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> |
| + | 95 | <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> | |
| 93 | 96 | ||
| 94 | == Further reading == | 97 | == Further reading == |