Author: Publisher:
ISBN:
Category : Code of federal regulations
Languages : en
Pages : 112
Book Description
Code of Federal Regulations
Author: Publisher:
ISBN:
Category : Code of federal regulations
Languages : en
Pages : 112
Book Description
Code of Federal Regulations
Author: Publisher:
ISBN:
Category : Administrative law
Languages : en
Pages : 1096
Book Description
Special edition of the Federal register. Subject/agency index for rules codified in the Code of Federal Regulations, revised as of Jan. 1 ...
FDA's catalog of information materials for the food and cosmetic industries
Author: Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised As of April 1 2012
Author: U. s. Government Printing OfficePublisher: Government Printing Office
ISBN: 9780160907197
Category : Law
Languages : en
Pages : 220
Book Description
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government.
Beyond the HIPAA Privacy Rule
Author: Institute of MedicinePublisher: National Academies Press
ISBN: 0309124999
Category : Computers
Languages : en
Pages : 334
Book Description
In the realm of health care, privacy protections are needed to preserve patients' dignity and prevent possible harms. Ten years ago, to address these concerns as well as set guidelines for ethical health research, Congress called for a set of federal standards now known as the HIPAA Privacy Rule. In its 2009 report, Beyond the HIPAA Privacy Rule: Enhancing Privacy, Improving Health Through Research, the Institute of Medicine's Committee on Health Research and the Privacy of Health Information concludes that the HIPAA Privacy Rule does not protect privacy as well as it should, and that it impedes important health research.
Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems
Author: Ashok KatdarePublisher: 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.
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2009
Author: Publisher: Government Printing Office
ISBN: 9780160828867
Category : Law
Languages : en
Pages : 220
Book Description
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government.
Information Materials for the Food and Cosmetic Industries
Author: Medical Product Regulatory Affairs
Author: John J. TobinPublisher: John Wiley & Sons
ISBN: 3527644717
Category : Science
Languages : en
Pages : 304
Book Description
Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field. Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and regulation in the USA. Other topics dealt with include CDER, CBER and marketing and manufacturing licenses, the ICH process and Good Laboratory/Clinical/Manufacturing Practices. Everything pharmacologists, bioengineers, pharma engineers, students in pharmacy and those working in the pharmaceutical industry need to know about medical regulatory affairs.
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2010
Author: Publisher: Government Printing Office
ISBN: 9780160853838
Category : Law
Languages : en
Pages : 220
Book Description
The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government.