Good Manufacturing Practices For Pharmaceuticals: A Plan For Total Quality Control From Manufacturer To Consumer: Fifth Edition, (drugs And The Pharmaceutical Sciences)
by D. Nally Joseph /
2000 / English / PDF
8.9 MB Download
Highlighting key issues and differences among GMPs of Europe,
Canada, and the WHO, this reference examines US law and
governmental policy affecting domestic and multinational
pharmaceutical manufacturing. The book recommend pragmatic ways to
interpret and comply with FDA CGMP regulation and related criteria.
They focus on geographical redistribution of manufacturing
facilities, accommodation of a diversity of regulatory and
statutory governance, adaptation to disparate human resources, and
new growth areas of manufacture and distribution of homeopathic
remedies and dietary supplements, in addition to the greater
quality control required of pharmacists and other authorized
dispensers.
Highlighting key issues and differences among GMPs of Europe,
Canada, and the WHO, this reference examines US law and
governmental policy affecting domestic and multinational
pharmaceutical manufacturing. The book recommend pragmatic ways to
interpret and comply with FDA CGMP regulation and related criteria.
They focus on geographical redistribution of manufacturing
facilities, accommodation of a diversity of regulatory and
statutory governance, adaptation to disparate human resources, and
new growth areas of manufacture and distribution of homeopathic
remedies and dietary supplements, in addition to the greater
quality control required of pharmacists and other authorized
dispensers.