Training Management
The operation and application of active medical devices is often subject to legal regulation.
LHNetEvent clearly incorporates the statutory basics within a training module.
When commissioning medical technical appliances, checks must be carried out by the manufacturer or authorised persons. Representatives are appointed and trained by the manufacturer. These officers are in turn responsible for the training of those persons who will use the medical devices.
The implementation of the functional test and training given by the responsible officer must be documented with the name and signature of all participants. Briefing of further persons can be carried out by the officer. In this case this training must also be documented by signature. These documents are to be made available to the regulators when required.
In any of the above training the following questions may arise.
- Who is trained in which area?
- What training has an employee?
- Who is commissioned for a certain type?
- In what areas is a particular employee authorized?
- What employee in a department is not trained in an area of activity and needs to make up the training?
These and many more complex questions can be answered with LHNetEvent training module, available from a number of sources over internet/intranet. Ordinarily, a single selection criterion is enough to obtain the desired information. Various permit documentation is available on this self-explanatory platform, saving much time in the collecting of permits.
Overview of functions
- Full accordance with legal requirements
- Documentation of manufacturer permits – individual or collective instructions possible
- Use of browsers
- Internet/Intranet use
- Fast and clear analysis for LHNetEvent and visual FM prepared lists for documentation and print
The LHNetEvent instruction module is applicable for the documentation of instructions in the area of ordinance on health and safety regulations for air equipment.