Document:EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011
From GxPlex
| Document information | |
|---|---|
| Reference | EU Eudralex - volume 4
GMP Guidelines Chapter 4 Jan-2011 |
| Validity area | EU |
| Scope(s) | G |
| Document name | Eudralex - volume 4
GMP Guidelines Chapter 4 |
| Version / Revision | Jan-2011 |
| Status | N.A. |
| Document type | Corpus of texts |
| Language(s) | EN |
| Description | EudraLex The Rules Governing Medicinal Products in the European Union Volume 4
Good Manufacturing Practice Medicinal Products for Human and Veterinary Use Chapter 4: Documentation |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
References
| Scope | Document part | Language | Preview | |
|---|---|---|---|---|
| EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011 4 | G | 4 | EN | Documentation Practices
4.7 Handwritten entries should be made in clear, legible, indelible way. […] 4.9 Any alteration made to the entry on a documen… |
