Development and quality control aspects
- In: C2 - Why is Dissolution Testing still needed? on Monday, 30 August 2010, 9:00-12:00
- At: Lisbon (Portugal) (2010)
- Type: Presentation
- By: SOUSA LOBO, José Manuel (University of Porto - Faculty of Pharmacy, Porto, Portugal)
- Abstract:
The way solid dosage forms release the active substances they contain has always been a main subject of research, and the relation between the release characteristics and the therapeutic activity of the dosage form was deeply studied. Following the growing importance of regulatory affairs concerning the manufacture and quality control of dosage
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Last update 28 September 2023