In Vitro Drug Release Testing of Veterinary Pharmaceuticals

Author:

Higgins-Gruber Shannon,Rathbone Michael J.,Brumfield Jay C.

Publisher

Springer US

Reference63 articles.

1. United States Pharmacopeia 34—National Formulary 29 (2011) <1088> In vitro and in vivo evaluation of dosage forms. United States Pharmacopeia Convention, Rockville, MD, pp 612–617

2. United States Pharmacopeia 34—National Formulary 29 (2011) <711> Dissolution. United States Pharmacopeia Convention, Rockville, MD, pp 278–284

3. Siewart M, Dressman J, Brown C, Shah V (2003) FIP/AAPS guidelines for dissolution/in vitro release testing of novel/special dosage forms. Dissolution Technol 10(1):6–15

4. Brown WE (2005) Compendial requirements of dissolution testing – European pharmacopoeia, United States pharmacopeia. In: Dressman J, Krämer J (eds) Pharmaceutical Dissolution Testing, 1st edn. Taylor & Francis, New York pp, pp 69–80

5. Kramer J, Grady LT, Gajendran J (2005) Historical development of dissolution testing. In: Dressman J, Krämer J (eds) Pharmaceutical Dissolution Testing, 1st edn. Taylor & Francis, New York pp, pp 1–37

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