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| DC Field | Value | Language |
|---|---|---|
| dc.date.accessioned | 2025-05-21T15:41:33Z | - |
| dc.date.available | 2025-05-21T15:41:33Z | - |
| dc.date.issued | 2008 | - |
| dc.identifier.uri | https://dlib.phenikaa-uni.edu.vn/handle/PNK/11926 | - |
| dc.description.abstract | This Guideline has been developed by the appropriate ICH Expert Working Group and has been subject to consultation by the regulatory parties, in accordance with the ICH Process. At Step 4 of the Process the final draft is recommended for adoption to the regulatory bodies of the European Union, Japan and USA. | vi |
| dc.language.iso | en | vi |
| dc.publisher | ICH | vi |
| dc.subject | Pharmaceutical quality system | vi |
| dc.subject | Q10 | vi |
| dc.title | Pharmaceutical quality system Q10 | vi |
| dc.type | Other | vi |
| Appears in Collections | ||
| BST Luật và các văn bản pháp luật | ||
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