Reference:WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth report -: Difference between revisions
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| | |has_document=Document:WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth report | ||
| | |module=4 | ||
| | |unit=4.2.2 | ||
| | |scope=G | ||
| | |doc_part=- | ||
| | |language=EN | ||
|entry_by=Florian Adragna | |||
|contributors= | |||
Β | |tags=TAG-00132-Goo-rst ++ TAG-00343-Doc-ten ++ TAG-00035-Man-odu | ||
|tags_display=[[Glossary:TAG-00132-Goo-rst|Good manufacturing practice]], [[Glossary:TAG-00343-Doc-ten|Documentation]], [[Glossary:TAG-00035-Man-odu|Manufacturing]] | |||
Β | |comment=GMP documentation principles | ||
|content=Annex 3: WHO good manufacturing practices: main principles for pharmaceutical products | |||
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Annex 3: WHO good manufacturing practices: main principles for pharmaceutical products | |||
[...] | [...] | ||
15. Documentation | 15. Documentation | ||
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When a document has been revised, the document management system should function in such a way as to prevent the inadvertent use of documents that have been superseded. | When a document has been revised, the document management system should function in such a way as to prevent the inadvertent use of documents that have been superseded. | ||
[...] | [...] | ||
}} | |||
Latest revision as of 13:50, 16 July 2026
| Document information | |
|---|---|
| Reference | WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth
report |
| Validity area | WHO |
| Scope(s) | G |
| Document name | WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS |
| Version / Revision | Forty-fifth
report |
| Status | N.A. |
| Document type | Other |
| Language(s) | EN |
| Description | WHO EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS
Forty-fifth repor |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 4 β Unit 4.2.2 |
| Scope | G |
| Document part | - |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Good manufacturing practice, Documentation, Manufacturing |
Content
Annex 3: WHO good manufacturing practices: main principles for pharmaceutical products [...] 15. Documentation [...] 15.6 Where documents require the entry of data, these entries should be clear, legible and indelible. Sufο¬cient space should be provided for such entries.
15.7 Any alteration made to a document should be signed and dated; the alteration should permit the reading of the original information. Where appropriate, the reason for the alteration should be recorded. [β¦] Annex 4: WHO guidelines on good manufacturing practices for blood establishments [β¦] 5.2 Document control [...] 5.2.1 Document management [β¦] When a document has been revised, the document management system should function in such a way as to prevent the inadvertent use of documents that have been superseded. [...]
