Draft Santa Rosa and San Jacinto Mountains National Monument Management Plan, and Draft Environmental Impact Statement PDF Download

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Category : Conservation of natural resources
Languages : en
Pages : 450

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Publisher: Oxford University Press, USA
ISBN: 9780199251759
Category : History
Languages : en
Pages : 348

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This title includes information and analysis on global small arms production, stockpiles and legal and illicit transfers, and a review of international, regional and national measures to address the issue of small arms proliferation.

Author: www.1clicktong.com
Publisher: Risk Management 1 Click Tong
ISBN:
Category : Technology & Engineering
Languages : en
Pages : 28

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1.1 This section of GB 6675 specifies the maximum limit requirements for the migration of elements such as antimony, arsenic, barium, cadmium, chromium, lead, mercury and selenium in the toy material and toy parts, the sampling method, and the preparation and extraction procedures for the test specimens. 1.2 The maximum limits for the migration elements specified in this section are applicable to the following toy materials: —Paints, lacquers, raw lacquer, inks, polymer coatings and similar coatings (see 8.1); —Polymers and similar materials include laminates whether enforced by textile or not, but exclude other textile and non-woven fabrics (see 8.2); —Paper and cardboard with maximum unit area of no more than 400 g/m2 (see 8.3); —Natural, artificial or synthetic fabrics (see 8.4); —Glass/ceramic/metallic materials except for lead fluxes used for electrical connection (see 8.5); —Other mass-colored materials, whether or not dyed (e. g. wood, fibreboard, cardboard, bone and leather)(see 8.6); —Materials that will leave traces (such as the graphite material in the pencil and the liquid ink in the pen)(see 8.7); —Soft molding materials including modeling clay and gels (see 8.8); —The pigment used in the toy, including paint, varnish, raw lacquer, vitreous powder, and other similar solid or liquid materials (see 8.9).1.3 The requirements of this section apply to the following toys, toy parts and toy materials (see C.2.1): —All toys intended for contact with food or mouth, cosmetic toys and writing implements belonging to the class of toys, regardless of age or recommended age identification. —All toys intended for or suitable for use in 72 months and below. —Accessible coating, no matter any age group or recommended applicable age identification. —Accessible liquids, creams and gels (e. g. liquid paints, modelling compounds), regardless of age group or recommended age identification. 1.4 The packaging material is not included in the scope of this section unless they are intended to be retained, such as boxes, containers, or unless they form part of a toy or are designed to have play value (see C.2.2). NOTE: Taking into account the normal and predictable behaviour of children, this section does not require certain toys and toy parts if they are clearly excluded the possibility of being sucked, foraged or swallowed due to their accessibility, function, mass, size or other characteristics. (e.g. a coating on a beam of a wobble device, and a tire of a toy bicycle, etc.)

Author:
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Category : Government publications
Languages : en
Pages : 742

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Category :
Languages : en
Pages : 732

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Category :
Languages : en
Pages : 450

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ISBN:
Category : Environmental impact statements
Languages : en
Pages : 624

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Author: Mark A. Abramson
Publisher: Rowman & Littlefield
ISBN: 9780742527973
Category : Business & Economics
Languages : en
Pages : 426

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Provides in-depth case studies of the "state" of e-government today. The book chronicles the "early days" of e-government and presents a collective snapshot in time as to where governments - at the federal, state, and local levels - are today as they continue their march toward e-government. Editors Abramson and Morin present a comprehensive "progress report" on e-government before a distinguished list of contributors discuss such varied topics as the quality of federal websites, technology and innovation in the State Department, online voting, and public-sector information security. Through grants for research and forums, The IBM Endowment for The Business of Government stimulates research and facilitates discussion on new approaches to improving the effectiveness of government at the federal, state, local, and international levels.

Author: Frederick M. Abbott
Publisher: Edward Elgar Publishing
ISBN: 1849801843
Category : Law
Languages : en
Pages : 319

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There is a strong argument that people throughout the world have a right to receive the medicines they need in an appropriate, affordable, and timely way. Global Pharmaceutical Policy describes the laws, policies, and customs relating to the development and provision of medicines, identifies their strengths and weakness, and then proposes global solutions for getting things better. Here is a masterpiece written in a clear and elegant style. Together, Dukes and Abbott have experience and insight that are unrivalled. Joe Collier, Emeritus Professor of Medicines Policy, St George s, University of London, UK Pharmaceuticals play a central role in health care throughout the world. The pharmaceutical industry is beset with difficulties as increasing research and development expenditure yields fewer new treatments. Public and private budgets strain under the weight of high prices and limited access. The world s poor see little effort to address diseases prevalent in less affluent societies, while the world s wealthy are overusing prescription drugs, risking their health and wasting resources. As the global economic crisis exacerbates pressure on health care budgets, a new presidential administration in Washington, DC has committed to broad health care reform. These circumstances form the backdrop for this extraordinarily timely examination of the global system for the development, production, distribution and use of medicines. The authors are acknowledged experts in the fields of pharmaceutical law and policy, with many years experience advising governments, multilateral organizations and policy-makers on issues involving innovation, access and use of medicines. Supported by a team of independent scientists, doctors and lawyers, they take an insightful look at the issues surrounding global regulation of the pharmaceutical sector, and offer pragmatic suggestions for reform. This book will be of interest to government policy-makers, members of industry, healthcare professionals, teachers, students and lawyers in the fields of public health, intellectual property and international trade.

Author:
Publisher:
ISBN:
Category : Environmental impact analysis
Languages : en
Pages : 782

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