Pharmaceutical Dosage Form Design

by A Sharma, YS Tanwar

The book “Pharmaceutical Dosage Form Design” is a unique organization of style that combines coverage of physical pharmacy and dosage form design. This text supplies new and must-have information regarding the excipients, preformulation studies, GMPs, validation procedure, ISO 9000, TQM, dissolution testing, bioequivalence studies, novel drug delivery systems, cosmetic manufacturing and quality control as well as packaging of dosage forms. The major objective of this edition is to serve as a textbook for graduate and postgraduate students in pharmaceutics. All the chapters are brief, clear and concise to provide students an understandable text and recent developments in the field. This book is comprised total 12 chapters. The first deals with the introduction to dosage forms. The second and third chapters discuss the pharmaceutical excipients and preformulation. The fourth chapter describes the quality management in pharmaceutical industry. The fifth and sixth chapter focuses on the dissolution testing of dosage forms, and bioavailability and bioequivalence studies. The seventh and eighth chapter discusses the stability testing of pharmaceuticals, and synthesis, properties and applications of polymers. The ninth chapter discusses an overview on prodrugs. The tenth and eleventh chapter focuses on the drug delivery systems and fundamentals of cosmetics. The final chapter deals with the packaging of dosage forms.

ADD TO FAVOURITES