That the AED is maintained and regularly tested according to the operation and maintenance guidelines set forth by the manufacturer, the American Heart Association, and the American Red Cross, and according to any applicable rules and regulations set forth by the governmental authority under the federal Food and Drug Administration and another other applicable state and federal authority.
A Routine Maintenance Program is developed by Emergency University which meets manufacturer guidelines. Tracking of routine maintenance dates and automated emails notifying of upcoming maintenance provided by EU Program Manager Database. EU staff comes in to site to perform maintenance functions and maintains compliance.
That the AED is checked for readiness after each use and at least once every 30 days. Records of these checks shall be maintained.
EU staff inspects the AED after each use. Company AED site manager performs checks monthly (or more frequently depending on manufacturer regulations. EU AED Program manager database tracks dates routine maintenance is performed and generates automatic reminder emails of upcoming maintenance. EU staff monitors compliance and notifies company AED site manager of non compliance.
For every AED unit acquired up to five units, no less than one employee per AED unit shall complete a training course in cardiopulmonary resuscitation and AED use that complies with the regulations adopted by the Emergency Medical Service Authority and the standards of the American Heart Association or the American Red Cross. After the first five AED units are acquired, one employee shall be trained beginning with the first AED unit acquired. Acquirers of AED units shall have trained employees who should be available to respond to an emergency that may involve the use of an AED unit during normal operating hours.
Emergency University provides CPR and manufacturer specific AED training which is developed in accordance with the guidelines published by the American Heart Association and ILCOR (International Liaison Committee On Resuscitation).
That there is a written plan that describes the procedures to be followed in the event of an emergency that may involve the use of an AED, to ensure compliance with the requirements of this section. The written plan shall include, but not be limited to, immediate notification of 911 and trained office personnel at the start of AED procedures.
EU staff, in conjunction with company designees, develops a site specific emergency response plan, AED use protocol, and AED policy and procedures. These documents are posted in the EU Program manager database as downloadable pdf files which can be easily accessed and printed at the local site. The Emergency Response plan includes both notification of the internal responders as well as timely notification of 911.
Notify an agent of the local EMS agency of the existence, location, and type of AED acquired.
Emergency University notifies the local EMS agency of the date acquired, manufacturer, and model of the AED and its location. Notification information is stored in the EU AED Program Manager database.
That any person who renders emergency care or treatment on a person in cardiac arrest by using an AED activates the emergency medical services system as soon as possible, and reports any use of the AED to the licensed physician and to the local EMS agency.
EU's AED Worksafe Program provides Medical Direction. Licensed Physicians review every use of the AED and EU notifies the local EMS agency of that use. A written report of the review is prepared and sent to the company's designee.
That there is involvement of a licensed physician in developing a program to ensure compliance with regulations and requirements for training, notification, and maintenance.
All AED response plans, policies and procedures, and protocols developed by EU are reviewed and approved by a licensed physician prior to implementation.