Contact Person : Smita; Last Date for the submission of abstract : Not Available ; Description : Webinar: One-Click Backup, Recovery, and Continuity https://www2.gotomeeting.com/register/324947474 Tue, Oct 9, 2012 10:00 AM - 10:30 AM PDT Join Quorum and learn about the only solution that …

Contact Person : Event Coordinator; Last Date for the submission of abstract : 41518; Description : Overview: This webinar is intended to assist practices develop the HIPAA Security Rule required incident response plan.

Contact Person : Event Coordinator; Last Date for the submission of abstract : Not Available ; Description : During this presentation, we will review the decision-making process and care planning roles of a nurse and how these roles and processes can be expanded to address the full lifetime of an i…

Contact Person : Event Coordinator; Last Date for the submission of abstract : Not Available ; Description : The introduction of new drugs and the ongoing researches on therapies directed at critical molecular targets require a good knowledge about the conduction of clinical trials.

Contact Person : Event Coordinator; Last Date for the submission of abstract : Not Available ; Description : E-mail has long been a staple of people's lives, but as we move into the new digital age, it seems everyone is moving to a new smart phone and wants to use it in all the incredible ways it c…

Contact Person : Event Coordinator; Last Date for the submission of abstract : Not Available ; Description : 45 CFR 46.111 (a)(2) states, "In evaluating risks and benefits, the IRB should consider only those risks and benefits that may result from the research (as distinguished from risks and benef…

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : cGMP regulations require that medical product manufactures define and control movement of materials, personnel, and waste to reduce the likelihood of mix-ups and contamination.

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : Device manufacturers are required to establish and maintain a medical device adverse event reporting system, commonly known as Medical Device Reporting. This webinar will demonstrate how to esta…

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application…

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : For workers who will be dealing with Quality Control testing and Process Validations it is very important to know some basic requirements for setting and dealing with specifications.

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : When the European Union's changes to the Medical Device Directive (MDD) went into effect in March 2010, it created a requirement for Clinical Evaluation.One of the new requirements has the devic…

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : Periodic Evaluation and Review of critical computer systems assures that the system is continuously operating within its validated state.The FDA expects periodic review & evaluation of computer …

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : The webinar is designed to provide the introductory information that a QC or manufacturing worker needs in order to understand the methods for comparing test results or measurements.

Contact Person : John Robinson; Last Date for the submission of abstract : Not Available ; Description : Clinical testing and studies of effectiveness are often needed to demonstrate that new medical devices are reasonably safe and effective. The participation of human subjects in these studies oft…