Handbook of Pharmaceutical Granulation Technology

Handbook of Pharmaceutical Granulation Technology
Author: Dilip M. Parikh
Publisher: CRC Press
Total Pages: 678
Release: 2016-04-19
Genre: Medical
ISBN: 1616310030

The Third Edition presents all pharmaceutical industry personnel and those in academia with critical updates on the recent advances in granulation technology and changes in FDA regulatory guidelines. Addressing precisely how these recent innovations and revisions affect unit operation of particle generation and granulation, this text assists the re

Handbook of Pharmaceutical Granulation Technology

Handbook of Pharmaceutical Granulation Technology
Author: Dilip M. Parikh
Publisher: CRC Press
Total Pages: 532
Release: 1997-06-17
Genre: Medical
ISBN: 9780824798826

Integrating the basic principles and industrial practices of pharmaceutical granulation production, this book discusses technologies and demonstrates cost-effective approaches to manufacturing solid-dosage forms with content uniformity and consistent physical properties while complying with regulatory requirements. Specialists from pharmaceutical companies, academia, and the U.S. Drug Regulatory Affairs agency address current and changing practices in industrial drug granulation production. Text, charts, figures, and photographs illustrate the pros and cons of diverse methods and technologies for accurately achieving strong bonding of particles in tablets and capsules.

Handbook of Pharmaceutical Granulation Technology

Handbook of Pharmaceutical Granulation Technology
Author: Dilip M. Parikh
Publisher: CRC Press
Total Pages: 905
Release: 2021-05-11
Genre: Medical
ISBN: 1000366383

Theoretical discussions covering granulation and engineering perspectives. Covers new advances in expert systems, process modelling and bioavailability Chapters on emerging technologies in particle engineering Updated Current research and developments in granulation technologies

Transport Processes in Pharmaceutical Systems

Transport Processes in Pharmaceutical Systems
Author: Gordon L. Amidon
Publisher: CRC Press
Total Pages: 746
Release: 1999-11-24
Genre: Science
ISBN: 0824746325

This cutting-edge reference clearly explains pharmaceutical transport phenomena, demonstrating applications ranging from drug or nutrient uptake into vesicle or cell suspensions, drug dissolution and absorption across biological membranes, whole body kinetics, and drug release from polymer reservoirs and matrices to heat and mass transport in freeze-drying and hygroscopicity. Focuses on practical applications of drug delivery from a physical and mechanistic perspective, highlighting biological systems. Written by more than 30 international authorities in the field, Transport Processes in Pharmaceutical Systems discusses the crucial relationship between the transport process and thermodynamic factors analyzes the dynamics of diffusion at liquid-liquid, liquid-solid, and liquid-cultured cell interfaces covers prodrug design for improving membrane transport addresses the effects of external stimuli in altering some natural and synthetic polymer matrices examines properties of hydrogels, including synthesis, swelling degree, swelling kinetics, permeability, biocompatibility, and biodegradability presents mass transfer of drugs and pharmacokinetics based on mass balance descriptions and more! Containing over 1000 references and more than 1100 equations, drawings, photographs, micrographs, and tables, Transport Processes in Pharmaceutical Systems is a must-read resource for research pharmacists, pharmaceutical scientists and chemists, chemical engineers, physical chemists, and upper-level undergraduate and graduate students in these disciplines.

Containment in the Pharmaceutical Industry

Containment in the Pharmaceutical Industry
Author: James P. Wood
Publisher: CRC Press
Total Pages: 274
Release: 2020-03-26
Genre: Medical
ISBN: 1000083020

Delivering an encompassing overview of the factors, varieties, and applications determining product containment, this concise reference provides authoritative information on containment processes. It reviews the historical context, definition, evolution, and application of containment technology, analyzes a variety of containment techniques in new

Pharmaceutical Experimental Design

Pharmaceutical Experimental Design
Author: Gareth A. Lewis
Publisher: CRC Press
Total Pages: 515
Release: 1998-09-10
Genre: Mathematics
ISBN: 0203508688

This useful reference describes the statistical planning and design of pharmaceutical experiments, covering all stages in the development process-including preformulation, formulation, process study and optimization, scale-up, and robust process and formulation development.Shows how to overcome pharmaceutical, technological, and economic constraint

Microbial Contamination Control in Parenteral Manufacturing

Microbial Contamination Control in Parenteral Manufacturing
Author: Kevin Williams
Publisher: CRC Press
Total Pages: 671
Release: 2004-05-20
Genre: Medical
ISBN: 113553621X

This reference surveys emerging trends, concepts, and procedures used in the characterization and control of contaminants; the sterile production of traditional drugs and biologics; the design, construction, and validation of new parenteral facilities; and the monitoring of clean environments-vividly illustrating the routes by which products, proce

Pharmaceutical Project Management

Pharmaceutical Project Management
Author: Anthony Kennedy
Publisher: CRC Press
Total Pages: 274
Release: 2008-03-17
Genre: Medical
ISBN: 104006292X

Encompassing the full spectrum of project management's role and responsibility encountered in the pharmaceutical industry, Pharmaceutical Project Management outlines the key objectives, risks, and challenges of each stage of the pharmaceutical lifecycle, from discovery and preclinical phases through clinical development, manufacturing, registration

Handbook of Pharmaceutical Analysis

Handbook of Pharmaceutical Analysis
Author: Lena Ohannesian
Publisher: CRC Press
Total Pages: 605
Release: 2001-11-09
Genre: Medical
ISBN: 0824741943

Exploring the analysis of pharmaceuticals, including polymorphic forms, this book discusses regulatory requirements in pharmaceutical product development and pharmaceutical testing. It covers methods of drug separation and procedures such as capillary electrophoresis for chromatographic separation of molecules. Additional topics include drug formulation analysis using vibrational and magnetic resonance spectroscopy and identification of drug metabolites and decomposition products using such techniques as mass spectrometry. The book provides more than 300 tables, equations, drawings, and photographs, and convenient, easy-to-use indices, facilitating quick access to each topic.

Biomarkers in Clinical Drug Development

Biomarkers in Clinical Drug Development
Author: John Bloom
Publisher: CRC Press
Total Pages: 312
Release: 2003-05-20
Genre: Medical
ISBN: 0824755197

Presenting applications in clinical development, pharmacokinetic/ pharmacodynamic modelling and clinical trial simulation, this reference studies the role of biomarkers in successful drug formulation and development.