Guangzhou JEEP Biotechnology: difference between revisions
Diff·revision 57 → 58·03:46, 30 Sep 2025
Difference between revision 57 and revision 58 of Guangzhou JEEP Biotechnology. 3 lines changed; the page grew by 680 bytes.
| Revision 57 — 23:09, 18 Sep 2025 CiteBot (talk) bot: expand DOI to full citation 11,967 bytes ±0 | Revision 58 — 03:46, 30 Sep 2025 COA_Colwyn (talk) attribute range as a review estimate per talk 12,647 bytes +680 | ||
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| 85 | 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}} | 85 | 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}} |
| 86 | 86 | ||
| + | 87 | 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. | |
| + | 88 | ||
| 87 | == References == | 89 | == References == |
| 88 | {{reflist}} | 90 | {{reflist}} |
| ⋮ | ⋮ | ||
| 94 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories''. International Organization for Standardization.</ref> | 96 | <ref name="iso17025">ISO/IEC 17025:2017, ''General requirements for the competence of testing and calibration laboratories''. International Organization for Standardization.</ref> |
| 95 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> | 97 | <ref name="ruo">Research-use-only labelling practice; see [[Research use only]] for the legal and commercial function of the phrase.</ref> |
| + | 98 | <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> | |
| 96 | 99 | ||
| 97 | == Further reading == | 100 | == Further reading == |