The Law of New Trials
Author | : Francis Hilliard |
Publisher | : |
Total Pages | : 760 |
Release | : 1866 |
Genre | : Appellate procedure |
ISBN | : |
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Author | : Francis Hilliard |
Publisher | : |
Total Pages | : 760 |
Release | : 1866 |
Genre | : Appellate procedure |
ISBN | : |
Author | : Francis Hilliard |
Publisher | : William s Hein & Company |
Total Pages | : 0 |
Release | : 1997 |
Genre | : New trials |
ISBN | : 9781575882062 |
Covers all aspects of the law of new trials, including the granting of a new trial, new trials in criminal cases, the jury in a new trial, and new evidence presented. Includes table of cases.
Author | : DALLAS. MACK |
Publisher | : |
Total Pages | : |
Release | : 2020 |
Genre | : |
ISBN | : 9780779896769 |
Author | : David Graham (Jr.) |
Publisher | : |
Total Pages | : 650 |
Release | : 1855 |
Genre | : New trials |
ISBN | : |
Author | : Miriam Hibel |
Publisher | : |
Total Pages | : 0 |
Release | : 2023 |
Genre | : Criminals |
ISBN | : 9781663357793 |
Author | : HardPress |
Publisher | : Hardpress Publishing |
Total Pages | : 768 |
Release | : 2013-01 |
Genre | : |
ISBN | : 9781313427890 |
Unlike some other reproductions of classic texts (1) We have not used OCR(Optical Character Recognition), as this leads to bad quality books with introduced typos. (2) In books where there are images such as portraits, maps, sketches etc We have endeavoured to keep the quality of these images, so they represent accurately the original artefact. Although occasionally there may be certain imperfections with these old texts, we feel they deserve to be made available for future generations to enjoy.
Author | : American Bar Association. House of Delegates |
Publisher | : American Bar Association |
Total Pages | : 216 |
Release | : 2007 |
Genre | : Law |
ISBN | : 9781590318737 |
The Model Rules of Professional Conduct provides an up-to-date resource for information on legal ethics. Federal, state and local courts in all jurisdictions look to the Rules for guidance in solving lawyer malpractice cases, disciplinary actions, disqualification issues, sanctions questions and much more. In this volume, black-letter Rules of Professional Conduct are followed by numbered Comments that explain each Rule's purpose and provide suggestions for its practical application. The Rules will help you identify proper conduct in a variety of given situations, review those instances where discretionary action is possible, and define the nature of the relationship between you and your clients, colleagues and the courts.
Author | : Francis Hilliard |
Publisher | : |
Total Pages | : 833 |
Release | : 1872 |
Genre | : Appellate procedure |
ISBN | : |
Author | : Graham |
Publisher | : |
Total Pages | : |
Release | : 1855 |
Genre | : |
ISBN | : |
Author | : Institute of Medicine |
Publisher | : National Academies Press |
Total Pages | : 236 |
Release | : 2015-04-20 |
Genre | : Medical |
ISBN | : 0309316324 |
Data sharing can accelerate new discoveries by avoiding duplicative trials, stimulating new ideas for research, and enabling the maximal scientific knowledge and benefits to be gained from the efforts of clinical trial participants and investigators. At the same time, sharing clinical trial data presents risks, burdens, and challenges. These include the need to protect the privacy and honor the consent of clinical trial participants; safeguard the legitimate economic interests of sponsors; and guard against invalid secondary analyses, which could undermine trust in clinical trials or otherwise harm public health. Sharing Clinical Trial Data presents activities and strategies for the responsible sharing of clinical trial data. With the goal of increasing scientific knowledge to lead to better therapies for patients, this book identifies guiding principles and makes recommendations to maximize the benefits and minimize risks. This report offers guidance on the types of clinical trial data available at different points in the process, the points in the process at which each type of data should be shared, methods for sharing data, what groups should have access to data, and future knowledge and infrastructure needs. Responsible sharing of clinical trial data will allow other investigators to replicate published findings and carry out additional analyses, strengthen the evidence base for regulatory and clinical decisions, and increase the scientific knowledge gained from investments by the funders of clinical trials. The recommendations of Sharing Clinical Trial Data will be useful both now and well into the future as improved sharing of data leads to a stronger evidence base for treatment. This book will be of interest to stakeholders across the spectrum of research-from funders, to researchers, to journals, to physicians, and ultimately, to patients.