Generic Drug Product Development

This book PDF is perfect for those who love Medical genre, written by Isadore Kanfer and published by CRC Press which was released on 19 April 2016 with total hardcover pages 334. You could read this book directly on your devices with pdf, epub and kindle format, check detail and related Generic Drug Product Development books below.

Generic Drug Product Development
Generic Drug Product Development
Author : Isadore Kanfer
File Size : 50,7 Mb
Publisher : CRC Press
Language : English
Release Date : 19 April 2016
ISBN : 9781420020021
Pages : 334 pages
Get Book

Generic Drug Product Development by Isadore Kanfer Book PDF Summary

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutica

Generic Drug Product Development

Generic Drug Product Development by Isadore Kanfer,Leon Shargel

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of

Get Book
Generic Drug Product Development

Generic Drug Product Development by Leon Shargel,Isadore Kanfer

In this era of increased pharmaceutical industry competition, success for generic drug companies is dependent on their ability to manufacture therapeutic-equivalent drug products in an economical and timely manner, while also being cognizant of patent infringement and other legal and regulatory concerns.Generic Drug Product Development: Solid Oral

Get Book
Generic Drug Product Development

Generic Drug Product Development by Leon Shargel,Isadore Kanfer

In this era of increased pharmaceutical industry competition, success for generic drug companies is dependent on their ability to manufacture therapeutic-equivalent drug products in an economical and timely manner, while also being cognizant of patent infringement and other legal and regulatory concerns. Generic Drug Product Development: Solid Oral Dosage Forms,

Get Book
Generic Drug Development Project Management

Generic Drug Development Project Management by Sandeep Narayan Patil, PMP

This is the first book in the series of three. These three books will be based upon the idea to tailor PMI’s Project Management methodologies to the typical pharmaceutical projects. This book includes generic drug development project in detail. It is specially designed for Project Managers, team members and

Get Book
Generic Drug Product Development

Generic Drug Product Development by Isadore Kanfer

The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be interchangeable. The demonstration of bioequivalence is an important component of

Get Book
Inhaled Pharmaceutical Product Development Perspectives

Inhaled Pharmaceutical Product Development Perspectives by Anthony J. Hickey

Inhaled Pharmaceutical Product Development Perspectives: Challenges and Opportunities describes methods and procedures for consideration when developing inhaled pharmaceuticals, while commenting on product development strategies and their suitability to support regulatory submission. It bridges the gap between the aspirations of scientists invested in new technology development and the requirements that must

Get Book
Generic Drug Product Development

Generic Drug Product Development by Isadore Kanfer,Leon Shargel

The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be interchangeable. The demonstration of bioequivalence is an important component of

Get Book
Pharmaceutical Quality by Design

Pharmaceutical Quality by Design by Sarwar Beg,Md Saquib Hasnain

Pharmaceutical Quality by Design: Principles and Applications discusses the Quality by Design (QbD) concept implemented by regulatory agencies to ensure the development of a consistent and high-quality pharmaceutical product that safely provides the maximum therapeutic benefit to patients. The book walks readers through the QbD framework by covering the fundamental

Get Book