Error Registering Phone 276
this section Academic Program Changes HASS Core Requirements Registration Academic Dates and Deadlines Automated Registration Waitlist Professional Development 2 Courses New Course and Topic Course Descriptions Add/drop CAPP reports Cross-registering at other schools Holds Independent study Time tickets Online registration error messages? Communication Intensive Requirement Undergraduate Research Program Grades & final exams Graduation Transfer Credit Study Abroad Registration error messages Error message Explanation Major Restriction The course is restricted to certain majors. Class Restriction The course is restricted to certain class(es), such as freshmen, sophomores, juniors, seniors, or graduate students Pre-Requisite You are required to complete another preparatory course before you can take the course for which you are attempting to register. Please refer to the Rensselaer Catalog for complete information on pre-requisite requirements. Closed The class or section for which you are attempting to register is full. Time Conflict You are attempting to register for courses whose meeting times overlap. If you are unable to register for any classes on-line, you may still petition to register for those courses by submitting an Authorization Form to the Registrar's office by the add deadline. Please refer to the Academic Calendar for specific dates. Academic calendar | Advising | Bursar | Co-Terminal Program | Catalog | First Year Experience | The Office of Graduate Education SIS | Student handbook | RPIALERT Emergency Notification System | RPI LMS | Veteran's Benefits Office of the Registrar, 2000 Level, Academy Hall, Rensselaer Polytechnic Institute (RPI), 110 Eighth Street, Troy, NY USA 12180 Phone: 518-276-6231 Fax: 518-276-6180 Why not change the world?SM is a service mark of Rensselaer Polytechnic Institute.
Sign in Pricing Blog Support Search GitHub This repository Watch 119 Star 1,394 Fork 1,337 phonegap-build/PushPlugin forked from bobeast/PushPlugin-deprecated Code Issues 371 Pull requests 69 Projects 0 Pulse Graphs New issue Can't get reg ID - callback from register function returns "OK" #276 Open Krysisx opened this Issue Jul 24, 2014 · 27 comments Projects None yet Labels None yet Milestone No milestone Assignees No http://registrar.rpi.edu/update.do?artcenterkey=22 one assigned 12 participants Krysisx commented Jul 24, 2014 I'm working on a cordova 3.5 application and I'm using this plugin for push notification. Here is my code: push_init: function(){ var SENDER_ID = "my GCM project number"; var pushNotification; var txt; var successHandler = function( result ) { navigator.notification.alert('Push: win -> ' https://github.com/phonegap-build/PushPlugin/issues/276 + result); }; var errorHandler = function( error ) { navigator.notification.alert('Push: error -> ' + error ); }; var push_android = function(e) { navigator.notification.alert('push_android() - connection established...'); switch( e.event ) { case 'registered': if ( e.regid.length > 0 ) { navigator.notification.alert("Regid " + e.regid); navigator.notification.alert('registration id = '+e.regid); } break; case 'message': navigator.notification.alert('message = '+e.message+' msgcnt = '+e.msgcnt); break; case 'error': navigator.notification.alert('GCM error = '+e.msg); break; default: navigator.notification.alert('An unknown GCM event has occurred'); break; } }; var onNotificationAPN = function( e ) { navigator.notification.alert('onNotificationAPN()'); }; try { pushNotification = window.plugins.pushNotification; if ( device.platform == 'android' || device.platform == 'Android' || device.platform == "amazon-fireos" ) { pushNotification.register( successHandler, errorHandler, { "senderID": SENDER_ID, "ecb": "push_android" } ); } else { pushNotification.register( successHandler, errorHandler, { "badge": "true", "sound": "true", "alert": "true", "ecb": "onNotificationAPN" } ); } } catch (error) { txt = "There was an error on this page.\n\n"; navigator.notification.alert(txt); } }, My problem is that
Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco http://www.fda.gov/RegulatoryInformation/Guidances/ucm094529.htm Products Regulatory Information Home Regulatory Information Search for FDA Guidance Documents Medical https://books.google.com/books?id=tPkFTVPcYR4C&pg=PA441&lpg=PA441&dq=error+registering+phone+276&source=bl&ots=JY9u1ssyky&sig=Za4kbhmQn6aBv8Fgx_5EWtQGTI4&hl=en&sa=X&ved=0ahUKEwiFoZXc19LPAhWh5IMKHe1IA98Q6AEIUDAI Device Reporting for Manufacturers Share Tweet Linkedin Pin it More sharing options Linkedin Pin it Email Print On July 9, 2013, the FDA issued a draft guidance titled, “Draft Guidance for Industry and Food and Drug Administration Staff; Medical Device Reporting for Manufacturers.” This draft guidance error registering document describes and explains the FDA regulation that addresses reporting and recordkeeping requirements applicable to manufacturers of medical devices for certain device-related adverse events. Please view the guidance for information on how to submit a comment to the docket for FDA’s consideration.PDF Printer Version(275 KB)DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Food and Drug AdministrationMedical Device error registering phone Reportingfor ManufacturersPrepared by Division of Small Manufacturers Assistance Office of Communication, Education, and Radiation ProgramsProject Officers: Bryan Benesch, Ron Parr and Timothy StockdaleMarch 1997DEPARTMENT OF HEALTH AND HUMAN SERVICES Public Health Service Food and Drug Administration Center for Devices and Radiological Health Rockville, Maryland 20850Note Concerning the March 27, 2000 Amendments to the MDR Regulation to Implement FDAMA ChangesThe FDA Modernization Act of 1997 (FDAMA) changes to medical device adverse event reporting (MDR) became effective on February 19, 1998. On January 26, 2000, we published in the Federal Register changes to the implementing regulations, 21CFR 803 and 804, to reflect these amendments in the act. Also, Part 804 was removed.The reporting changes are:Medical device manufacturers, importers, and distributors are no longer required to submit an annual certification statement.Domestic distributors no longer have to submit MDR reports, but they must continue to maintain records of adverse events.Importers continue to be subject to the remaining requirements of the MDR regulation, 21 CFR 803.User facilities now submit a report annually instead of semi-annually.The MDR Rule c
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