Download or read book Effective Environmental Assessments written by Charles Eccleston and published by CRC Press. This book was released on 2016-04-19 with total page 489 pages. Available in PDF, EPUB and Kindle. Book excerpt: Although upwards of 50,000 Environmental Assessments (EA) are prepared annually, the focus of the National Environmental Policy Acts (NEPA) Regulations is clearly on defining requirements for preparing environmental impact statements. Surprisingly, until now, there has been no authoritative and comprehensive guide on how to prepare Environmental As

Download or read book Preparing NEPA Environmental Assessments written by Charles Eccleston and published by CRC Press. This book was released on 2012-05-08 with total page 307 pages. Available in PDF, EPUB and Kindle. Book excerpt: Although upwards of 50,000 environmental assessments (EAs) are prepared annually-compared to some 500 environmental impact statements (EISs)-the focus of U.S. National Environmental Policy Act (NEPA) regulations is on defining requirements for preparing EISs. Written by Charles Eccleston and J. Peyton Doub, who have established themselves among the

Download or read book The NEPA Planning Process written by Charles H. Eccleston and published by John Wiley & Sons. This book was released on 1999-01-18 with total page 426 pages. Available in PDF, EPUB and Kindle. Book excerpt: Designed to save hours of painstaking research while minimizing costs and risk of litigation, it integrates critical information from hundreds of sources - including the Council on Environmental Quality (CEQ)'s NEPA regulations and guidance, presidential and EPA directives, case law, recent research from nationally recognized experts, and the professional experiences of NEPA practitioners.

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Download or read book Capillary Electrophoresis Methods for Pharmaceutical Analysis written by Satinder Ahuja and published by Elsevier. This book was released on 2011-08-09 with total page 546 pages. Available in PDF, EPUB and Kindle. Book excerpt: Capillary electrophoresis (CE) is a powerful analytical technique that is widely used in research and development and in quality control of pharmaceuticals. Many reports of highly efficient separations and methods have been published over the past 15 years. CE offers several advantages over high-pressure or high-performance liquid chromatography (HPLC). These include simplicity, rapid analysis, automation, ruggedness, different mechanisms for selectivity, and low cost. Moreover, EC requires smaller sample size and yet offers higher efficiency and thus greater resolution power over HPLC. These characteristics are very attractive in research and development, even more so in pharmaceutical quality control (QC) and stability monitoring (SM) studies. This book will provide busy pharmaceutical scientists a complete yet concise reference guide for utilizing the versatility of CE in new drug development and quality control.- Provides current status and future developments in CE analysis of pharmaceuticals.- Explains how to develop and validate methods.- Includes major pharmaceutical applications including assays and impurity testing.

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