http://events.boxesandarrows.com Thu, 03 May 2012 12:10:39 GMT http://events.boxesandarrows.com/events/1884 http://events.boxesandarrows.com/events/1884 This 90-minute webinar on sampling plans using ANSI/ASQ Z1.9 will explain the methods in Z1.9 and shows how to use it in a more modern setting (using simple statistical calculators). Thu, 03 May 2012 12:10:39 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1883 http://events.boxesandarrows.com/events/1883 This 90-minute presentation will discuss a structured way to mitigate risks with minimum cost. You will learn how to use FMEA to effectively estimate and assess risks in your medical device. Thu, 03 May 2012 12:07:25 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1882 http://events.boxesandarrows.com/events/1882 This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices. Thu, 03 May 2012 11:57:35 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1881 http://events.boxesandarrows.com/events/1881 This 90-minute webinar on device corrections and removals will clarify your obligations for corrections and removals under Part 806 of the FDA regulations. Thu, 03 May 2012 11:50:05 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1880 http://events.boxesandarrows.com/events/1880 This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA's tougher position. Thu, 03 May 2012 11:47:05 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1879 http://events.boxesandarrows.com/events/1879 This webinar on alarms in patient monitoring devices will show how you can address FDA concerns regarding alarm standards and safety. Thu, 03 May 2012 11:42:24 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1877 http://events.boxesandarrows.com/events/1877 This webinar on Trial Master File (TMF) for clinical research sites will show how you can create an FDA compliant TMF to ensure that it will pass inspection by FDA investigators and QA Auditors. Thu, 03 May 2012 10:38:27 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1876 http://events.boxesandarrows.com/events/1876 This webinar on issue detection and escalation in clinical trial settings will review the responsibilities of sponsors, investigators, IRB in clinical trial setting to maintain compliance. Thu, 03 May 2012 10:34:15 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1875 http://events.boxesandarrows.com/events/1875 This webinar will help you understand how non-IND clinical trials at non-US locations can be used successfully to support an IND/IDE or a marketing approval application. Thu, 03 May 2012 10:27:06 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1874 http://events.boxesandarrows.com/events/1874 This webinar on clinical trial audit/ inspection preparedness will discuss in detail about applicable regulatory and sponsor requirements, guidelines and SOPs. Thu, 03 May 2012 10:21:08 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1873 http://events.boxesandarrows.com/events/1873 This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial. Thu, 03 May 2012 10:07:48 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1872 http://events.boxesandarrows.com/events/1872 This webinar on IND and IDE Application management will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial. Thu, 03 May 2012 09:57:09 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1871 http://events.boxesandarrows.com/events/1871 We will review the latest inspection statistics released from FDA, discuss how to prepare for an FDA Inspection, Thu, 26 Apr 2012 15:01:13 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1870 http://events.boxesandarrows.com/events/1870 The topic aims to address and compare the requirements of SOX against the Dodd-Frank legislation and contrast how they differ clearly in purpose and objectives. Thu, 26 Apr 2012 14:59:06 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1869 http://events.boxesandarrows.com/events/1869 Find out what HHS OCR is likely to ask you if you are selected for an audit, and what you'll have to have prepared already when they do. Thu, 26 Apr 2012 14:56:38 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1868 http://events.boxesandarrows.com/events/1868 Short and quick overview of the Part 11 regulation; detailed description of HOW TO prepare for an FDA inspection when and where Part 11 is in scope or the scope of the inspection Thu, 26 Apr 2012 14:54:28 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1867 http://events.boxesandarrows.com/events/1867 By lowering the import risks to your suply chain would lead to fewer Customs inspections and delays to your freight. The reduce lead times would enhance cost savings. Thu, 26 Apr 2012 14:49:33 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1866 http://events.boxesandarrows.com/events/1866 Learn and understand the rules for international terms of sale; save pages of contract information by use of the proper rule. Thu, 26 Apr 2012 14:45:54 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1865 http://events.boxesandarrows.com/events/1865 Medical device firms need to be aware of the benefits of compliance as well as the dangers of inadequate complaint handling. Thu, 26 Apr 2012 14:42:52 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1859 http://events.boxesandarrows.com/events/1859 RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance at Mumbai Thu, 26 Apr 2012 12:12:03 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1858 http://events.boxesandarrows.com/events/1858 Current and future compliance professionals, lenders, loan originators, board of directors, senior management. Anyone responsible for the development, marketing, and sales of bank products . Thu, 26 Apr 2012 12:03:50 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1857 http://events.boxesandarrows.com/events/1857 The subject of risk compliance and 'are you prepared' is being discussed far more frequently (using platforms like webinars and white-paper downloads) Thu, 26 Apr 2012 12:00:19 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1852 http://events.boxesandarrows.com/events/1852 Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel Tue, 17 Apr 2012 05:37:43 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1851 http://events.boxesandarrows.com/events/1851 DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel Tue, 17 Apr 2012 05:34:47 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1847 http://events.boxesandarrows.com/events/1847 Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel Tue, 17 Apr 2012 05:22:08 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1839 http://events.boxesandarrows.com/events/1839 Two days with some of the world’s top UX, IA, and IxD pros. Fluxible’s format mixes hands-on workshops with informative presentations, tours of leading global businesses, and loads of fun! Thu, 29 Mar 2012 15:12:56 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1835 http://events.boxesandarrows.com/events/1835 Statistics for the Non-Statistician - US Seminar 2012 at Washington DC Wed, 28 Mar 2012 09:18:13 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1833 http://events.boxesandarrows.com/events/1833 HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties - US Seminar 2012 at Boston Wed, 28 Mar 2012 09:04:16 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1763 http://events.boxesandarrows.com/events/1763 Four day user experience conference - 2 days of workshops, 2 days of conference Fri, 03 Feb 2012 04:41:51 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1756 http://events.boxesandarrows.com/events/1756 Join experts in the fields of design, mobile, gaming, usability, strategy, content, multimedia, and film in Big D. Fri, 20 Jan 2012 03:05:17 GMT events@boxesandarrows.com http://events.boxesandarrows.com/events/1753 http://events.boxesandarrows.com/events/1753 UX Week is the premier user experience design conference. Design professionals from all over the world gather for four days of community, inspiration and skills building. Mon, 09 Jan 2012 23:54:39 GMT events@boxesandarrows.com