نتایج جستجو برای: regulatory authority

تعداد نتایج: 209871  

Journal: :Carbon Balance and Management 2009
Bryan K Mignone Matthew D Hurteau Yihsu Chen Brent Sohngen

BACKGROUND One controversial issue in the larger cap-and-trade debate is the proper use and certification of carbon offsets related to changes in land management. Advocates of an expanded offset supply claim that inclusion of such activities would expand the scope of the program and lower overall compliance costs, while opponents claim that it would weaken the environmental integrity of the pro...

Journal: :Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians 2013
John D Eisemann Jeanette R O'Hare Kathleen A Fagerstone

Several fertility control agents have recently been registered with the U.S. Environmental Protection Agency for management of wildlife or other free-ranging animals. The registration of GonaCon Immunocontraceptive Vaccine for use in white-tailed deer (Odocoileus virginianus) and OvoControl for use in Canada geese (Branta canadensis) and pigeons (Columba livia) has caused state wildlife and lan...

2013

This document is protected under national and international copyright law and treaties. This document and any accompanying material are for use only by the regulatory authority to which it has been submitted by Monsanto Company and only in support of actions requested by Monsanto Company. Any other use, copying, or transmission, including internet posting, of this document and the materials des...

2013
Neal L Benowitz Jack E Henningfield

Nicotine is highly addictive and is primarily responsible for the maintenance of cigarette smoking. In 1994, Benowitz and Henningfield proposed the idea of federal regulation of the nicotine content of cigarettes such that the nicotine content of cigarettes would be reduced over time, resulting in lower intake of nicotine and a lower level of nicotine dependence. When nicotine levels get very l...

2001
F. Balda

In recent years Risk Analysis has become increasingly important for any kind of project for both personnel and equipment safety assessments. Many divisional projects must respect the rules imposed by the French regulatory authority (INB) and the requirements of applicable international standards. This document proposes a systematic approach for the setting up of a complete Risk Analysis, and it...

Journal: :British journal of clinical pharmacology 2016
Michael Eddleston Adam F Cohen David J Webb

Over the past 10 years, thousands of first-into-human (FIH) clinical trials have been performed in Europe, with few severe adverse events (SAEs). Each has received detailed prior safety review at both the local clinical research facility and at national drug regulatory authority level. The recent fatal SAE in the BIA-102474-101 clinical trial shows the limitations of this process. Although crit...

2014
Luis Guijarro Vicent Pla Jose R. Vidal Jorge Martinez-Bauset Matjaz Perc

Spectrummanagement based on private commons is argued to be a realistic scenario for cognitive radio deployment within the current mobile market structure. A scenario is proposed where a secondary entrant operator leases spectrum from a primary incumbent operator. The secondary operator innovates incorporating cognitive radio technology, and it competes in quality of service and price against t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Aram J K Calhoun Jessica S Jansujwicz Kathleen P Bell Malcolm L Hunter

Vernal pools are far more important for providing ecosystem services than one would predict based on their small size. However, prevailing resource-management strategies are not effectively conserving pools and other small natural features on private lands. Solutions are complicated by tensions between private property and societal rights, uncertainties over resource location and function, dive...

Journal: :Journal of veterinary pharmacology and therapeutics 2004
P L Toutain P Lees

In veterinary drug development procedures, pharmacokinetic (PK) and pharmacodynamic (PD) data have generally been established in separate, parallel studies to assist in the design of dosage schedules for subsequent evaluation in clinical trials. This review introduces the concept of PK/PD modelling, an approach in which PK and PD data are generated in the same study, and used to derive numerica...

2017
Arthur Caplan

This paper examines how water quality trading interacts with nonpoint-source abatement cost sharing (e.g., as currently practiced by the National Resource Conservation Service through its Environmental Quality Incentives Program (EQIP)) to promote the participation of nonpoint sources in a water quality market; participation that has thus far been noticeably lacking nationwide. As such, an idea...

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