Get Free Ebook Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP
The benefits to take for reviewing the publications Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP are involving boost your life quality. The life quality will not only concerning exactly how significantly knowledge you will certainly get. Also you review the enjoyable or enjoyable books, it will certainly help you to have enhancing life high quality. Really feeling enjoyable will certainly lead you to do something perfectly. Furthermore, the e-book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP will certainly offer you the driving lesson to take as a good need to do something. You could not be pointless when reviewing this publication Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP
Get Free Ebook Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP
Use the advanced innovation that human creates this day to discover the book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP quickly. But initially, we will ask you, just how much do you like to read a book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP Does it consistently up until finish? For what does that book check out? Well, if you actually enjoy reading, try to check out the Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP as one of your reading collection. If you only reviewed guide based upon demand at the time and also incomplete, you need to try to such as reading Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP initially.
When some individuals taking a look at you while checking out Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP, you may feel so happy. But, as opposed to other individuals feels you must instil in yourself that you are reading Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP not due to that reasons. Reading this Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP will certainly provide you more than people admire. It will overview of understand more than the people staring at you. Even now, there are lots of resources to knowing, reading a publication Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP still comes to be the front runner as a wonderful method.
Why need to be reading Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP Once again, it will depend upon just how you really feel as well as consider it. It is definitely that one of the advantage to take when reading this Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP; you could take more lessons directly. Also you have actually not undergone it in your life; you can gain the encounter by reading Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP And now, we will certainly present you with the on the internet book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP in this web site.
What sort of publication Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP you will choose to? Now, you will certainly not take the published book. It is your time to get soft data book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP instead the published documents. You could appreciate this soft file Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP in whenever you anticipate. Also it remains in expected area as the various other do, you can review the book Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP in your device. Or if you really want a lot more, you can continue reading your computer or laptop computer to obtain full screen leading. Juts locate it right here by downloading the soft data Medical Device Development: Regulation And Law, By Jonathan S. Kahan, Hogan Lovells US LLP in link page.
Medical Device Development: Regulation and Law, 2014 Edition, is the ''must-have'' resource for the novice or veteran medical device regulatory affairs professional. This practical reference provides the most comprehensive and updated analysis of US medical device and diagnostics development and approval requirements anywhere. Since the 2009 edition of this book, new device legislation has been enacted and FDA has issued over a dozen or more important new guidances. The 2014 edition features in-depth analysis of these developments, and addresses how emerging developments and trends are reshaping medical device and combination product regulations in the US. The 2014 edition of this popular and authoritative resource reviews and analyzes the following critical developments since the 2009 edition: * Update on all the new provisions of the Food and Drug Administration Safety and Improvement Act of 2012 (FDASIA). * New statutory provisions and guidances related to device reclassification, humanitarian devices, the CDRH appeal process, Section 522 postmarket surveillance, and custom devices. * New statutory provisions and guidances related to mobile medical apps and medical device software, including medical data software systems. * Updates on the new organizational structure of CDRH, including revisions to the structure of the Office of Device Evaluation the Office of Compliance, and the Office of In Vitro Diagnostics and Radiological Health. * Changes to the 510(k) premarket notification process, including new policies on split predicates, when a device cannot be found to be SE, and the new priority review guidance. * Changes to the pre-submission process, including the end of the pre-IDE process and the birth of the Q-sub. * New guidances on FDA s Refusal to Accept policies relating to 510(k)s, PMA s, and pre-submissions. * Update on the investigational device exemption process, including new guidances on early feasibility studies, FDA decisions for IDE investigations, design considerations for pivotal clinical device investigations, and good laboratory practices. * Changes to the premarket approval application process, including birth of the e-copy and modifications to the advisory panel process. * New policies and guidances concerning in vitro diagnostic products, including the new guidances on Research Use Only (RUO)/Investigational Use Only (IUO) products, and in vitro companion diagnostics. * Update on device compliance issues, including the 2013 draft medical device reporting guidance and recall procedures relating to product enhancements. * New guidances and cases relating to combination products incorporating medical devices.
- Sales Rank: #61011 in Books
- Published on: 2014-03-01
- Binding: Hardcover
- 622 pages
Review
Great book for a beginner learning about process, or an experienced practitioner in the field. I used prior addition, until i realized it was updated - i testify on matters of value in the field of medical devices, and nothing helps the court understand faster - than a text book you can cite documenting the process of a 510(k) application or a PMA! --Richard Mackenzie, Amazon Verified Purchase
I recently acquired a copy of Jonathan Kahan s book entitled Medical Device Development: Regulation and Law, in its most recent edition. I have been in the regulatory affairs profession for over 23 years now, and can easily navigate websites and references to find the information I need. However, as I was reviewing a recent FDA proposed rule, I found myself repeatedly reaching out to the book as all the information I needed was compiled and easily found in one place, organized by topic, with all needed legislative and regulatory references. Mr. Kahan has done an admirable job in creating this book, and I am thankful to have it on my desk for easy reference when needed. --Tamima Itani, Ph.D., FRAPS, RAC MSVP, Global Regulatory Affairs and Regulatory Compliance, Boston Scientific
About the Author
The book is written by Jonathan S. Kahan, Partner, Hogan Lovells US LLP in Washington, D.C. Jon is a co-director of the firm s food, drug, medical device, and agriculture group, and has been practicing in FDA law for 40 years. Jon is also an Adjunct Professor at the George Washington University Law School teaching medical device law. His practice focuses primarily on assisting medical device companies in navigating the U.S. Food and Drug Administration (FDA) regulatory process. He also has an extensive practice in combination products, which includes combinations of drugs, devices, and biologics. In addition to the daily counseling of clients in FDA-related matters, he represents many clients in administrative hearings and trials, and in the federal courts. Jon has published numerous law review and other articles concerning FDA regulatory issues.
Most helpful customer reviews
2 of 2 people found the following review helpful.
Excellent, readable resource
By Susan Cook
Thorough review of the latest regulations, practices and thinking by the FDA. The book indicates the areas where there is still ongoing debate and lets the reader know the regulation at the time of printing, then provides information for finding if there are new updates since the printing. I like that the book is not fully pro FDA - it objectively discusses FDA actions and history of the evolution of the current regulations. I was not looking forward to having to read this book for a Medical Device class, but now have found it interesting and even engrossing to read. This is one of those books that I will use as a go-to guide for anything related to medical device regulation.
0 of 0 people found the following review helpful.
Comprehensive resource
By D. Coral
Many changes have occurred since the 2009 edition. This latest update keeps on top of these recent changes including "guidances related to mobile medical apps and medical device software, including medical data software systems" driven by all the new technology (e.g. iPads). It is very interesting reading as well. This is a must-have on your shelf if you are involved in any aspect of medical device regulation.
0 of 0 people found the following review helpful.
Good reference, simplifies and summarizes FDA.gov information on Medical Devices
By Tate
Good book for references especially if you are new to the medical device industry, need a refresher, and/or if you need the FDA website simplified and summarized for you.
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP PDF
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP EPub
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP Doc
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP iBooks
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP rtf
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP Mobipocket
Medical Device Development: Regulation and Law, by Jonathan S. Kahan, Hogan Lovells US LLP Kindle
Tidak ada komentar:
Posting Komentar