Author:
Publisher:
ISBN:
Category : Medicine
Languages : en
Pages : 360
Book Description
USP, NF.
USP 33 NF 28
Author: United States Pharmacopeial Convention
Publisher:
ISBN: 9781889788883
Category :
Languages : en
Pages : 668
Book Description
Publisher:
ISBN: 9781889788883
Category :
Languages : en
Pages : 668
Book Description
Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems
Author: Ashok Katdare
Publisher: CRC Press
ISBN: 1420004131
Category : Medical
Languages : en
Pages : 474
Book Description
To facilitate the development of novel drug delivery systems and biotechnology-oriented drugs, the need for new, yet to be developed, and approved excipients continues to increase. Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems serves as a comprehensive source to improve understanding of excipients and forge potential new avenues for regulatory approval. This book presents detailed, up-to-date information on various aspects of excipient development, testing, and technological considerations for their use. It addresses specific details such as historical perspective, preclinical testing, safety, and toxicology evaluation, as well as regulatory, quality, and utility aspects. The text also describes best practices for use of various functional excipients and extensive literature references for all topics.
Publisher: CRC Press
ISBN: 1420004131
Category : Medical
Languages : en
Pages : 474
Book Description
To facilitate the development of novel drug delivery systems and biotechnology-oriented drugs, the need for new, yet to be developed, and approved excipients continues to increase. Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems serves as a comprehensive source to improve understanding of excipients and forge potential new avenues for regulatory approval. This book presents detailed, up-to-date information on various aspects of excipient development, testing, and technological considerations for their use. It addresses specific details such as historical perspective, preclinical testing, safety, and toxicology evaluation, as well as regulatory, quality, and utility aspects. The text also describes best practices for use of various functional excipients and extensive literature references for all topics.
Usp38-Nf33
Author: United States Pharmacopeial Convention
Publisher:
ISBN: 9781936424320
Category : Medicine
Languages : en
Pages :
Book Description
Publisher:
ISBN: 9781936424320
Category : Medicine
Languages : en
Pages :
Book Description
The Code of Federal Regulations of the United States of America
Author:
Publisher:
ISBN:
Category : Administrative law
Languages : en
Pages : 1088
Book Description
The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government.
Publisher:
ISBN:
Category : Administrative law
Languages : en
Pages : 1088
Book Description
The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government.
USP 33 NF 28
Author: United States Pharmacopeial Convention
Publisher:
ISBN: 9781889788883
Category :
Languages : en
Pages : 491
Book Description
Publisher:
ISBN: 9781889788883
Category :
Languages : en
Pages : 491
Book Description
Contemporary Drug Information
Author: Claude J. Gaebelein
Publisher: Lippincott Williams & Wilkins
ISBN: 9780781782807
Category : Medical
Languages : en
Pages : 388
Book Description
This innovative textbook teaches the basics of drug information, literature evaluation, and biostatistics, and relates these topics to evidence-based pharmaceutical care. Readers will learn what to look for in studies, how to critique them, and how to apply them in clinical pharmacy practice. A major focus is critical appraisal of evidence derived from different types of studies—cases, cohorts, surveys, randomized controlled clinical trials, pharmacoeconomic studies, and systematic reviews. Concluding chapters discuss clinical decision-making using evidence from studies.
Publisher: Lippincott Williams & Wilkins
ISBN: 9780781782807
Category : Medical
Languages : en
Pages : 388
Book Description
This innovative textbook teaches the basics of drug information, literature evaluation, and biostatistics, and relates these topics to evidence-based pharmaceutical care. Readers will learn what to look for in studies, how to critique them, and how to apply them in clinical pharmacy practice. A major focus is critical appraisal of evidence derived from different types of studies—cases, cohorts, surveys, randomized controlled clinical trials, pharmacoeconomic studies, and systematic reviews. Concluding chapters discuss clinical decision-making using evidence from studies.
Handbook of Pharmaceutical Granulation Technology
Author: Dilip M. Parikh
Publisher: CRC Press
ISBN: 1000366383
Category : Medical
Languages : en
Pages : 905
Book Description
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
Publisher: CRC Press
ISBN: 1000366383
Category : Medical
Languages : en
Pages : 905
Book Description
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
Nutraceutical and Functional Food Regulations in the United States and Around the World
Author: Debasis Bagchi
Publisher: Academic Press
ISBN: 0080920527
Category : Law
Languages : en
Pages : 462
Book Description
Globalization of the nutraceutical and functional food industries presents significant challenges, not the least of which is the regulatory variance between countries active in the marketplace. Nutraceutical and Functional Food Regulations in the United States and Around the World has been written by eminent experts in the field with the specific intention of addressing these important considerations. Beginning with insights into the scope, importance and growing opportunities in these industries, the book demonstrates the global scenario on the acceptance and demand for nutraceuticals and functional foods. It explores the regulatory hurdles and claim substantiation of these foods and dietary supplements, as well as the intricate aspects of manufacturing procedures. Including regulations from South America, Canada, European Union, Australia, New Zealand, Africa, Japan, Korea, China, India and Southeast Asia as well as the United States, Nutraceutical and Functional Food Regulations in the United States and Around the World provides a valuable resource for understanding the key considerations of operating in this rapidly expanding area. - Overview of nutraceutical and functional food regulations around the world - Discusses the important of GRAS status and DSHEA regulations - Provides insight on quality manufacturing techniques, cGMP and standardized analytical techniques - Includes salient features on overcoming regulatory hurdles - Addresses the importance of safety, efficacy and human clinical studies for worldwide acceptance - Highlights anti-terrorism safety assurance through traceability - Explores the significance of intellectual property, trademark and branding on marketing
Publisher: Academic Press
ISBN: 0080920527
Category : Law
Languages : en
Pages : 462
Book Description
Globalization of the nutraceutical and functional food industries presents significant challenges, not the least of which is the regulatory variance between countries active in the marketplace. Nutraceutical and Functional Food Regulations in the United States and Around the World has been written by eminent experts in the field with the specific intention of addressing these important considerations. Beginning with insights into the scope, importance and growing opportunities in these industries, the book demonstrates the global scenario on the acceptance and demand for nutraceuticals and functional foods. It explores the regulatory hurdles and claim substantiation of these foods and dietary supplements, as well as the intricate aspects of manufacturing procedures. Including regulations from South America, Canada, European Union, Australia, New Zealand, Africa, Japan, Korea, China, India and Southeast Asia as well as the United States, Nutraceutical and Functional Food Regulations in the United States and Around the World provides a valuable resource for understanding the key considerations of operating in this rapidly expanding area. - Overview of nutraceutical and functional food regulations around the world - Discusses the important of GRAS status and DSHEA regulations - Provides insight on quality manufacturing techniques, cGMP and standardized analytical techniques - Includes salient features on overcoming regulatory hurdles - Addresses the importance of safety, efficacy and human clinical studies for worldwide acceptance - Highlights anti-terrorism safety assurance through traceability - Explores the significance of intellectual property, trademark and branding on marketing
Usp39-Nf34
Author: United States Pharmacopeial Convention
Publisher:
ISBN: 9781936424443
Category :
Languages : en
Pages :
Book Description
Publisher:
ISBN: 9781936424443
Category :
Languages : en
Pages :
Book Description