Validation of Free Formaldehyde Determination Method in DT Vaccine and Tetanus Toxoid Antigen
Validation is a Good Manufacturing Practice principle that proves any procedure, process, method, equipment, material, activity, or system actually leads to the expected results. This study validates the method for the determination of free formaldehyde in biological products (including the diphther...
Kaydedildi:
| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Razi Vaccine and Serum Research Institute
2023-06-01
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| Seri Bilgileri: | Archives of Razi Institute |
| Konular: | |
| Online Erişim: | https://archrazi.areeo.ac.ir/article_128771_4312a4881cbb47c87f6e8d37acbf592c.pdf |
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