Pn544 User Manual Is Only Available Under Nda

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Information contained in this manual is subject to change without notice and does not represent a commitment on the part of Arturia. The software described in this manual is provided under the terms of a license agreement or non-disclosure agreement. The software license agreement specifies the terms and conditions for its lawful use. Dec 22, 2016  Question Information on the NFC chipset/daemon Question. Ifixit comes to the conclusion that the NFC chipset is an NXP PN544, I can't find a datasheet on it only an overview https. It's only available under NDA. I found a couple people saying that. Mar 25, 2016 I want know how to get something about PN544 restrict documents, currently I have new project use IMX6 with a SIP module (built-in PN544), need debug NFC stack and something RF settings of PN544. If need sign NDA, please tell me how to doing this. Page 1 BC 278CLT 1 0 B A N D, 1 0 0 C H A N N E L S C A N N E R. FULLY PROGRAMMABLE. FULL FREQUENCY LCD READOUT. ALARM CLOCK. AM/FM RADIO.; Page 2 Changes or modifications to this product not expressly approved by Uniden, or operation of this product in any way other than as detailed by this Reference Guide, could void your authority to operate this product. Of this manual. Note: The JN516x SDKs for some protocols have moved to the ‘BeyondStudio for NXP’ toolchain. The installation of these SDKs and the toolchain is described in the BeyondStudio for NXP Installation and User Guide (JN-UG-3098). Caution: Before installing an SDK described in this manual, you must remove any previous JN51xx SDK.

  1. Pn544 User Manual Is Only Available Under Nda Free
  2. Pn544 User Manual Is Only Available Under Nda Form
  • 1General NFC resources

General NFC resources

Here are some NFC resources:

Introduction to Linux NFC

  • NFC on Linux (PDF) - presentation by Samuel Ortiz, November 2012
    • Video of presentation at ELC Europe 2012 (Barcelona, November 9th)
  • Linux NFC Subsystem (PDF) - presentation from ELC Europe 2011 by Lauro Ramos Venancio and Samuel Ortiz
    • Video of presentation at ELC Europe 2011 (Prague, November)
  • Enabling Mobile Payments on Linux (video) - presentation by Samuel Ortiz, September 2013

NFC news and articles

finding which devices use which chips

  • http://en.wikipedia.org/wiki/List_of_NFC-enabled_mobile_devices
    • Would be a great resource, if it was populated
  • http://www.shop4nfc.com/nfc-compatibility-chart - List of different devices and the NFC chips they use
    • But they seem to have the wrong chip for some Sony devices
  • This seems to be a handy site for finding out what chips a particular product uses:

Devices that use the NXP PN544

  • Huawei Ascend U8651
  • Motorola Droid Razr
  • Nokia C7 (labeled as NXP 44501)[1]
  • Nokia N9 (labeled as NXP 44501)
  • Samsung Galaxy S II (selected models, labeled as NXP 44501)[2]
  • Samsung Galaxy mini 2 S6500 (labeled as NXP 44501)[3]
  • Samsung Galaxy Note 3 (earlier models)
  • Moto X 1st generation (labeled as NXP 44701)[4]

Devices that use the NXP PN65

  • HTC One (and One X, One X+, and One XL)[5]
  • Nexus 7 Tablet
  • Samsung Galaxy S III[6]
  • Sony Xperia Z[7]
Only

Devices that use the Broadcom BCM20793M

Pn544 user manual is only available under nda 2018
  • LG Nexus 5 [8][9]
  • Galaxy S4
  • Nexus 7 (2013) Tablet

Devices that use the Broadcom BCM20793S

  • Nexus 4 tablet[10]
  • Nexus 10 tablet

Devices that use the Broadcom BCM20794

  • Samsung Galaxy Note 3 (SM-N9009)[11]

Vendors of Secure Elements

ST MicroelectronicsNXPSecure InsideInfineon

Vendors of NFC chipsets

  • NXP[12]
    • PN544 C1, PN544 C2, PN544 C3**
    • PN546**
    • PN547 C1**, PN547 C2**
    • PN548 C2**
    • PN65N (PN544 C2 + SmartMX secure element)
    • PN65O** (PN544 C3 + SmartMX secure element)
    • PN65T** (PN547 C2 + SmartMX secure element)
    • PN66T** (PN548 C2 + SmartMX secure element)

Note, ** means that recent firmware versions are qualified (by MasterCard or VISA) for payments with HCE (Host-based Card Emulation) and SE (Secure Element).[13]

  • Broadcom
    • BCM20793M
    • BCM20793S (includes a secure element)
    • BCM20794
  • Secure Inside
    • MicroRead

News

Google supports Host Card Emulation (HCE), which eliminates the need for a secure element componentin the mobile device itself. SE services can be provided by the network ('cloud'), or by trusted software.This support was announced for the KitKat (4.4) version of Android.

Software Interface

  • http://open-nfc.org/wp/ - Open-NFC project
    • This project appears to be a multi-OS driver for MicroRead hardware (but with a HAL for other chips)
  • libnfc
    • open-source project for accessing NFC features from user-space
  • Android APIs
    • Official API resources: http://developer.android.com/reference/android/nfc/package-summary.html
    • Android NFC guide: http://developer.android.com/guide/topics/connectivity/nfc/index.html
    • Tutorial for basic tag reading from Android: http://mifareclassicdetectiononandroid.blogspot.se/2011/04/reading-mifare-classic-1k-from-android.html

Footnotes

  1. ↑http://sebastianschaper.net/index.php/archives/37
  2. ↑http://www.nfc.cc/nfc-phones/samsung-galaxy-s-ii-nfc-i9100/
  3. ↑https://www.youtube.com/watch?v=QXFTHe82ZPk
  4. ↑https://de.ifixit.com/Teardown/Motorola+Moto+X+Teardown/16867#s51669
  5. ↑https://forum.xda-developers.com/showthread.php?t=2282045
  6. ↑https://www.ifixit.com/Teardown/Samsung+Galaxy+S+III+Teardown/9391#s36088
  7. ↑http://www.persoapp.de/forums/topic/kompatibilitat-der-mobilen-persoapp-mit-sony-xperia-l-c2105/
  8. ↑http://www.geek.com/android/nexus-5-could-debut-a-more-open-google-wallet-that-works-with-all-phones-1575354/
  9. ↑http://arstechnica.com/gadgets/2013/11/ifixit-easily-tears-apart-the-decidedly-high-end-nexus-5/
  10. ↑http://www.nfcbrief.com/2013/08/google-completes-broadcom-transition.html
  11. ↑https://wikidevi.com/wiki/Samsung_Galaxy_Note_III_%28SM-N9009%29
  12. ↑{{url=http://mastercard-mobilepartner.com/docs/NFC%20FW%20NXP%20v2%209_160328.pdf title=Recommended NFC configurations publisher=MasterCard date=2015-06-25 accessdate=2017-01-17}}
  13. ↑Template:Url=https://technologypartner.visa.com/Download.aspx?id=360
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Introduction

For decades, the regulation and control of new drugs in the United States has been based on the New Drug Application (NDA). Since 1938, every new drug has been the subject of an approved NDA before U.S. commercialization. The NDA application is the vehicle through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing in the U.S. The data gathered during the animal studies and human clinical trials of an Investigational New Drug (IND) become part of the NDA.

The goals of the NDA are to provide enough information to permit FDA reviewer to reach the following key decisions:

  • Whether the drug is safe and effective in its proposed use(s), and whether the benefits of the drug outweigh the risks.
  • Whether the drug's proposed labeling (package insert) is appropriate, and what it should contain.
  • Whether the methods used in manufacturing the drug and the controls used to maintain the drug's quality are adequate to preserve the drug's identity, strength, quality, and purity.

The documentation required in an NDA is supposed to tell the drug's whole story, including what happened during the clinical tests, what the ingredients of the drug are, the results of the animal studies, how the drug behaves in the body, and how it is manufactured, processed and packaged. The following resources provide summaries on NDA content, format, and classification, plus the NDA review process:

Resources for NDA Submissions

The following resources have been gathered to provide you with the legal requirements of a new drug application, assistance from CDER to help you meet those requirements, and internal NDA review principles, policies and procedures.

Guidance Documents for NDAs

Guidance documents represent the Agency's current thinking on a particular subject. These documents are prepared for FDA review staff and applicants/sponsors to provide guidelines to the processing, content, and evaluation/approval of applications and also to the design, production, manufacturing, and testing of regulated products. They also establish policies intended to achieve consistency in the Agency's regulatory approach and establish inspection and enforcement procedures. Because guidances are not regulations or laws, they are not enforceable, either through administrative actions or through the courts. An alternative approach may be used if such approach satisfies the requirements of the applicable statute, regulations, or both. For information on a specific guidance document, please contact the originating office.

For the complete list of CDER guidances, please see the Guidance Index. For information on a specific guidance document, please contact the originating office.

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Guidance documents to help prepare NDAs:.

Laws, Regulations, Policies and Procedures

The mission of FDA is to enforce laws enacted by the U.S. Congress and regulations established by the Agency to protect the consumer's health, safety, and pocketbook. The Federal Food, Drug, and Cosmetic Act is the basic food and drug law of the U.S. With numerous amendments, it is the most extensive law of its kind in the world. The law is intended to assure consumers that foods are pure and wholesome, safe to eat, and produced under sanitary conditions; that drugs and devices are safe and effective for their intended uses; that cosmetics are safe and made from appropriate ingredients; and that all labeling and packaging is truthful, informative, and not deceptive.

Code Of Federal Regulations (CFR)

The final regulations published in the Federal Register (daily published record of proposed rules, final rules, meeting notices, etc.) are collected in the CFR. The CFR is divided into 50 titles which represent broad areas subject to Federal regulations. The FDA's portion of the CFR interprets the Federal Food, Drug and Cosmetic Act and related statutes. Section 21 of the CFR contains all regulations pertaining to food and drugs. The regulations document all actions of all drug sponsors that are required under Federal law.

Pn544 User Manual Is Only Available Under Nda Free

  • 21CFR Part 314 - Applications for FDA Approval to Market a New Drug or an Antibiotic Drug.
CDER's Manual of Policies and Procedures (MaPPs)

These documents are approved instructions for internal practices and procedures followed by CDER staff to help standardize the new drug review process and other activities. MaPPs define external activities as well. All MaPPs are available for the public to review to get a better understanding of office policies, definitions, staff responsibilities and procedures.

MaPPS of particular interest to NDA applicants

Prescription Drug User Fee Act (PDUFA)

On November 21, 1997, The President signed the Food and Drug Administration Modernization Act of 1997. This legislation includes authorization for FDA to continue to collect three types of user fees from applicants who submit certain new drug and biological product applications. FDA was first authorized to collect user fees under the Prescription Drug User Fee Act (PDUFA) of 1992.

NDA Forms and Electronic Submissions

  • Form FDA-356h. Application to Market a New Drug, Biologic, or An Antibiotic Drug For Human Use
  • Form FDA-3397. User Fee Cover Sheet
  • Form FDA-3331. New Drug Application Field Report
  • For more information on electronic submissions, see Electronic Regulatory Submissions and Review Helpful Links.

Advisory Committees

Advisory committees provide independent advice and recommendations to the FDA on scientific and technical matters related to the development and evaluation of products regulated by the Agency. CDER requests advice from advisory committees on a variety of matters, including various aspects of clinical investigations and applications for marketing approval of drug products. Committee members are scientific experts such as physician-researchers and statisticians, as well as representatives of the public, including patients. Although the committees provide recommendations to the Agency, final decisions are made by FDA. Autodesk autocad 2015 user manual pdf.

  • CFR 21 Part 14 Public Hearing Before a Public Advisory Committee. Detailed description of advisory committees from the Code of Federal Regulations.
  • Guidance for Industry: Advisory Committees. Includes information on membership, conflict of interest, scheduling, and action on recommendations.
  • Advisory Committee Meeting Calendar. Several dates have been set aside by CDER advisory committees for possible future meetings. The subject matter and location of the meetings (if they are held) will be published in the Federal Register in the month prior to the meeting date.

Related Topics

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Pn544 User Manual Is Only Available Under Nda Form