FIP Guidelines for Dissolution Testing of Solid Oral Products (Final Draft, 1995)
- 1 October 1996
- journal article
- research article
- Published by Springer Nature in Drug Information Journal
- Vol. 30 (4) , 1071-1084
- https://doi.org/10.1177/009286159603000424
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- In vitro/in vivo correlations: Scientific implications and standardisationEuropean Journal of Drug Metabolism and Pharmacokinetics, 1993
- Influence of Higher Rates of Agitation on Release Patterns of Immediate‐Release Drug ProductsJournal of Pharmaceutical Sciences, 1992
- Effects of Sinker Shapes on Dissolution ProfilesJournal of Pharmaceutical Sciences, 1989
- Food-Induced Theophylline Release/Absorption Changes from Controlled-Release Formulations: A Proposed In Vitro ModelDrug Development and Industrial Pharmacy, 1988
- Simulation of Physiological pH - Time Profile in In Vitro Dissolution Study: Relationship Between Dissolution Rate and Bioavailability of Controlled Release Dosage FormDrug Development and Industrial Pharmacy, 1988
- Influence of a High Fat Breakfast on the Bioavailability of Theophylline Controlled-Release Formulations: An In Vitro Demonstration of an In Vivo ObservationJournal of Pharmaceutical Sciences, 1986
- Drug dissolution studies in milk using the automated flow injection serial dynamic dialysis techniqueInternational Journal of Pharmaceutics, 1986
- Advances in Dissolution Technology: Design, Pros and ConsDrug Development and Industrial Pharmacy, 1986
- Effect of Sampling Probe Size on Dissolution of Tableted Drug SamplesJournal of Pharmaceutical Sciences, 1981
- New Method for Calculating the Intrinsic Absorption Rate of DrugsJournal of Pharmaceutical Sciences, 1968