1. Formulation of dermatologic vehicles;Barry,1983
2. Rheology of dermatological vehicles;Barry,1983
3. The clinical relevance of in vitro investigations for percutaneous absorption;Barry,1985
4. Extemporaneous compounding: Promotional and legal aspects;Fassett;Am Pharmacy,1984
5. Food and Drug Administration Title 21 Code of Federal Regulations. Part 21—Current good manufacturing practice for finished pharmaceuticals. United States.