Selasa, 18 Desember 2012

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Inquests and Inquiries: a practitioner's guide is the only text that examines practice and procedure of the coroner's court from the point of view of practitioner acting for the bereaved. It has been updated to include changes introduced in the Coroners and Justice Act 2009 as well as the Coroners Regulations and Rules introduced in 2013.

  • Sales Rank: #7454316 in Books
  • Published on: 2014-03-18
  • Dimensions: 8.27" h x 1.50" w x 5.83" l,
  • Binding: Paperback
  • 768 pages

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1 of 1 people found the following review helpful.
Promoting the rights of bereaved people....
By Phillip Taylor MBE
[[VIDEOID:moAWIGYOKMJPDS]]
THE DEFINITIVE GUIDE ON INQUESTS
NOW IN A NEW THIRD EDITION

An appreciation by Phillip Taylor MBE and Elizabeth Taylor of Richmond Green Chambers

Writing in the foreword to the new third edition of this outstanding and well established practitioner's guide, HHJ Peter Thornton QC, the Chief Coroner for England and Wales, defines the function and value of coroners and therefore inquests.

`Coroners perform an important service,' he points out, adding that this public service is `first and foremost for bereaved families... and secondly, for the wider public good'.

Explaining that the service is at least 800 years old, he mentions the significant changes that have recently taken place within it, referring to the `new statutory regime governing the powers and duties of coroners'. It is anticipated that one of the positive results -- including a number of highly important procedural changes -- will be to create a more modern and efficient service aimed at lessening distress for families and also allowing coroners to concentrate on more difficult cases.

For practitioners involved in this sensitive area, an understanding of case law and theory is of course important. But even more important is knowing what to do when faced with the complexities of an inquest -- and this is where this book is especially helpful. It is a plain-speaking guide to the practice and procedure of the coroners' court.

Particularly noteworthy is that the book is written by a team of authors whose expertise has been honed and tested in the arena of actual experience. No mere theorists these. Dedicating the book to `all bereaved families touched by the inquest process,' each of them has worked on high profile and often controversial cases. Leslie Thomas for example (named Legal Aid Lawyer of the Year 2012 and who, by happy coincidence, took Silk on the day this book was launched) has worked on Hillsborough, as has Adam Straw whose experience has included the cases of Jean Charles de Menezes and Alexander Litvinenko.

Daniel Machover, a specialist in international human rights law, is currently Chair of INQUEST, the organisation dedicated to upholding the rights of bereaved families within the coronial system. Danny Friedman QC, a specialist in crime, human rights, public law and international humanitarian law, also writes the human rights chapter in `Archbold: Criminal Pleading, Evidence and Practice.'

In researching, compiling and publishing this book, the LAG (Legal Action Group) perpetuates its noble tradition of producing detailed and thorough guides to the law that are not only of direct practical use for practitioners, but accessible as well, to interested and concerned members of the general public.

Indisputably authoritative and up-to-date, the book is an accessible and valuable resource, as it also contains extensive tables of cases, statutes, statutory instruments and international conventions, plus four appendices that include legislation, precedents and forms. Anyone involved in any or all matters relating to inquests, should certainly consider this book indispensable as you will see it in courtrooms across the country.

The publication date is cited as at February 2014.

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Senin, 17 Desember 2012

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El Poder de Ahorrar te ayuda alcanzar la libertad financiera y te gu�a para que puedas lograr todos tus objetivos econ�micos y financieros con metodolog�as de ahorro: Visualizar tus metas, preparar tus finanzas hasta alcanzar el equilibrio econ�mico, conocer las herramientas m�s factibles para que tus ahorros crezcan, descubrir los mejores trucos para adquirir una gran capacidad de ahorro hasta alcanzar la visi�n de ser autosuficientes. No es s�lo una gu�a, no es s�lo es un manual. Es el cambio de paradigma de las finanzas personales usado como palanca de cambio a trav�s del ahorro para lograr nuestras metas, nuestra independencia econ�mica y la libertad financiera. Este libro te va a entregar EL PODER para conseguir todo lo que te propongas para lograr una vida libre, f�cil y sostenible.

  • Sales Rank: #7070952 in Books
  • Published on: 2012-09-24
  • Original language: Spanish
  • Dimensions: 9.00" h x .34" w x 6.00" l,
  • Binding: Paperback
  • 142 pages

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0 of 0 people found the following review helpful.
Buen libro a pesar que esta enfocado en la econom�a ...
By Amazon Customer
Buen libro a pesar que esta enfocado en la econom�a de estados unidos, me hubiese gustado que viera la situaci�n real de chile!!..

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Minggu, 16 Desember 2012

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  • Sales Rank: #13432127 in Books
  • Brand: Brand: Liverpool University Press
  • Published on: 1998
  • Original language: English
  • Number of items: 1
  • Dimensions: 9.21" h x 6.14" w x .0" l, 1.07 pounds
  • Binding: Paperback
  • 288 pages
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  • Sales Rank: #1480799 in Books
  • Brand: Brand: McGraw-Hill Humanities/Social Sciences/Languages
  • Published on: 2003-07-28
  • Original language: English
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Minggu, 09 Desember 2012

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Development of FDA-Regulated Medical Products: A Translational Approach, Second Edition, by Elaine Whitmore

Translating promising discoveries and innovations into useful, marketable medical products demands a robust process to guide nascent products through a tangle of scientific, clinical, regulatory, economic, social, and legal challenges. There are so many human and environmental elements involved in shepherding medical advances from lab to launch that the field of medical product development has been referred to as an ecosystem. The purpose of this book is to help provide a shared foundation from which cross-functional participants in that ecosystem can negotiate the product development labyrinth and accomplish the goal of providing both groundbreaking and iterative new medical products. The book is intended for anyone in industry, the public sector, or academia regardless of functional specialty, workplace, or seniority who is interested in medical product development. The years since the publication of the previous edition of this book have seen profound changes in the actions and attitudes of patients, insurers, manufacturers, and the Food and Drug Administration regarding the streamlining of medical product development and approval. What those years have not seen is a concomitant increase in innovative treatments with profound benefits to patients. Despite enormous investments in research by both private and public sources and a surge in scientific and technological advances, new medical products barely trickle into the marketplace. For a variety of reasons, applied sciences necessary for medical product development are not keeping pace with the tremendous advances in basic sciences. Not surprisingly, industry and academia are under substantial pressure to transform discoveries and innovations from the laboratory into safe and effective medical products to benefit patients and improve health. This evolution from bench to bedside has become known as translational research and development, and this approach is what this book illuminates.

  • Sales Rank: #465230 in Books
  • Brand: Whitmore, Elaine
  • Published on: 2012-02-22
  • Original language: English
  • Dimensions: 9.25" h x 6.25" w x 1.00" l, 1.10 pounds
  • Binding: Hardcover
  • 256 pages
Features
  • Used Book in Good Condition

Most helpful customer reviews

4 of 4 people found the following review helpful.
Finally, Someone gets it right!
By Joseph P. Sener
I have been working in medical device design and design assurance for over 10 years. I have been having the fight and argument with management that "of course it is harder to do it right than not but your current approach has really not worked so well!!!

Elaine Whitmore really gets this right. The one paragraph that really got me ranting is on page 80: "A significant challenge for anyone working in product development in the healthcare field, especially with medical devices where stringent controls and requirements are a relatively new issue, is overcoming a bad attitude." "...The point is that quality regulations are not going to go away, and those responsible for healthcare product development will have to lead the charge to keep up the momentum in their organizations."

I am going to have to buy several copies of this for my clients!

3 of 3 people found the following review helpful.
Essential guide for medical product management, investors, scientists and engineers
By David M. Wiseman
Dr. Whitmore exposes a raw nerve too long protected by the bubble that has been the biotech boom of the last 20 or so years. In her opening salvo she observes "there is no lack of innovation or shortage of important scientific discoveries in this country, but our ability to transform scientific advances into new and effective medical products has been disappointing."

In attempting to pinpoint the reason for the gap between expectations and actual productivity, Dr. Whitmore rounds up the usual suspects of outdated clinical trial models, and an inefficient system of regulation, but reserves the focus of her scrutiny on the way in which investment money is spent and in the product development process itself.

The days when Big Pharma or Big Device companies funded their own internal R&D have dwindled, the mammoths now choosing for the most part to outsource their innovation and early stage product development to a larger, more diverse pool of start-ups whose investors assume much of the risk. Although this system provides the opportunity for more innovation in small companies unconstrained by Big Pharma bureaucracy, the focus of risk imposes pressures on the start-up either to cut corners or to abandon prematurely perfectly good avenues of innovation.

There has to be a better way.

Invoking the term "Translational Research", i.e. the methods used to accelerate the path of a scientific discovery from the bench to the patient, Dr. Whitmore dissects the entire process, charting the path needed to ensure success and, more importantly needed to avoid the "Valley of Death", that graveyard of innovations that have failed to implant, gestate or deliver.

Dr. Whitmore's subtext is that there are no shortcuts, but there are smarter ways to navigate the path to success. Her guidebook not only provides beacons for the scientist, engineer or innovator, but a guidebook for investors and management who can better understand the challenges and more appropriately balance their risks and expectations.

The style is clear and concise and achieves its goal of helping to "provide a shared foundation from which cross-functional participants...can negotiate the product development labyrinth and accomplish the goal of providing both groundbreaking and iterative new medical products."

Should be required reading for anyone in the industry.

1 of 1 people found the following review helpful.
A Must Read for any Healthcare Professional
By Tyler
The updated version of this book provides new insight into the development of medical products in changing times, where regulation now takes longer to pass through than development. This is really a beginners overview of the process, so if you work in the industry some of the chapters may seem a bit simple and lacking in content. Overall it is a great read for anyone (especially healthcare providers) that want to know more about how medical devices are regulated.

See all 3 customer reviews...

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