Generic drug product development
An edition of Generic drug product development (2007)
International Regulatory Requirements for Bioequivalence
By Leon Shargel,Isadore Kanfer
Publish Date
2016
Publisher
Taylor & Francis Group
Language
eng
Pages
310
Description:
subjects: Drugs, Drug development, Testing, Law and legislation, Pharmaceutical industry, Pharmaceutical technology, Medical / Pharmacology, Pharmacology, Medical, Medical / Nursing, Generic drugs, Drugs, generic substitution, Drugs, dosage, Solid dosage forms, Generic Drugs, Standards, Pharmaceutical Chemistry, Drug Approval, Tablets, Dosage forms, Therapeutic equivalency, Dosage Forms