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TOPICS : 04- EUROPEAN PHARMACOPOEIA & INTERNATIONAL HARMONISATION / 01- General Chapters and Monographs  / 08- PHARMACOTECHNOLOGY 

• 01. When should I apply Chapter 2.9.40 ‘UNIFORMITY OF DOSAGE UNITS’?

• 02. Dissolution test for solid dosage forms: what is the quantity Q?

• 03. Dissolution test for solid dosage forms: I don’t understand how to calculate the acceptance criteria. Could you give an example?


 
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