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From Lorman Education Services
Risk Management in Telephone Triage: Lessons Learned From Telephone Triage Litigation
BenefitsThe telephone, once used merely as an appointment scheduling device, has become an integral part of provider-patient interactions. Research indicates that approximately 20 to 28 percent of all primary health care is handled over the telephone. However, without proper training and accountability, telephone triage can result in improper diagnosis and management as well as legal liability.
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Risk Management in Telephone Triage: Lessons Learned From Telephone Triage Litigation
BenefitsThe telephone, once used merely as an appointment scheduling device, has become an integral part of provider-patient interactions. Research indicates that approximately 20 to 28 percent of all primary health care is handled over the telephone. However, without proper training and accountability, telephone triage can result in improper diagnosis and management as well as legal liability.
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From GlobalCompliancePanel
FDA Requirements for Device Labeling Development Contents Distribution and Changes - Webinar By GlobalCompliancePanel
This webinar is designed for those who perform, supervise, manage, audit, or oversee the creation, approval, control of labels and labeling.
Tuesday, December 6, 2011
10: 00 AM PST | 01: 00 PM EST
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Purchasing and Supplier Controls in the Medical Device Industry - Webinars GlobalCompliancePanel
This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.
Wednesday, November 16, 2011
10: 00 AM PST | 01: 00 PM EST
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FDAs New Draft Guidance on Medical Device Changes and the 510k
This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011. It will examine the broad range of issues to be considered by a company when reviewing 1) A series of minor changes or 2) one major change to an existing product having an existing 510(k), for the need for a
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Validating Radiation Sterilization for Medical Device Industries- WEBINARS BY GCP
Gamma and E-Beam radiation has used for sterilization of medical devices for over 50 years. Both methods are validated following the same principles and standards. This webinar will provide an overview of the requirements to validate medical devices for both Gamma and E-Beam sterilization.
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Device Changes FDA Changes and the 510k - Webinar by GlobalCompliancePanel
The majority of medical devices are cleared for marketing in the U. S. by the FDA under the 510(k) process.
The FDA holds companies responsible for filing new 510(k)s when one change is major enough to impact safety / effectiveness, or when a series of lesser changes finally reach the "tipping point". This is a major headache. How can companies make that determination? How can they trigger such
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From Matsya Technologies
Job Oriented Training in LAMPLinuxApacheMysqlPHPJavaJ2EECCUnixLinuxkernel internalsDevice driversShell ProgrammingPerlPythonOrac
Job Oriented Training in LAMP(Linux, Apache, Mysql, PHP),Java/ J2EE, C,C++,Unix/ Linux(kernel internals/ Device drivers),Shell Programming, Perl, Python, Oracle, PL/ SQL with Placement
Matsya Technologies operates not-for-profit Free/ Open Source Software Laboratory (FOSS LAB) at Silicon Valley of India - Bangalore.
The FOSS LAB is involved in consultancy & training on LAMP(Linux, Apache,
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From Michael Burlacu Yoga Studio
CHAIR YOGA Yoga for Seniors
The classes are a perfect blend of physical postures, breathing techniques, concentration and relaxation.
The Yoga practice will increase your energy level, strength, balance and flexibility; it helps focus the mind, and slows down the ageing process.
All exercises will be performed sitting on a chair or using a chair as an assistive device.
10 classes, each class will be one hour long.
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