Nowadays, the need for control over manufacturing environment is too high. However, as the need for manufacturing control has risen gradually, it has attracted a need for better equipment management used in measuring and controlling manufacturing processes. The best way of managing such equipment is by calibrating and maintaining the machine correctly.
Many managers find themselves in difficulties since the number of equipment they manage may be proliferating something that leads to increased responsibilities; consequently, they end up having their resources reducing. The idea of implementing commercial off-the-shelf calibration – management software, is one of the most suitable for resource minimization.
If you need an easy way of Validated Calibration Management System, you may opt to justify a move away from legacy calibration management system. In case you need ammunition for CMS justification, below are some few significant advantages you can grasp quickly:
Computer records tend to be better than paper records since they will remain in one place occupying a small space, unlike paper records that can easily be misplaced and occupy considerable space.
GxP Calibration Management system will be responsible for answer question such as; how you are notified of pending calibration or preventive maintenance events. Whether you remember all of them, you miss some of those, or you miss time to time, whether calibration or maintenance events ever occur without being documented.
Having a good calibration system, it will be in a position to schedule calibration and give you notifications on their due date. Every piece of data is stored securely in an accessible way to those who may need it. On top of that, downtime will be highly reduced since your equipment is maintained and even calibrated on time.
Comparing routine calibration with finding out of tolerance instruments in a field you will see that routine calibration is much cheaper and will have reduced waste due to improved product quality.
Compliance With Standards And Regulations
ISO requires that calibration is done thoroughly and timely similarly to Food and Drug Administration regulations. Your calibration management system should meet these requirements.
The real work kicks off once the decision of implementing a calibration management system has been initiated. One requires proper planning and effort and following some few steps carefully – this way the approach does not need to be a challenging activity.
User Requirement Specifications
The actual manufacturing process becomes easier once one conducts proper research, follows the required steps carefully and makes a good investment in design and planning a process known as the pre-manufacturing process. It is a rule that still applies to select and implement a Validated Calibration Management Software.
One of the mistakes many managers do while implementing a CMS is starting the process by searching CMS vendors online. Every different feature attracts a variable cost for worldwide vendors. You should begin the process by identifying specific requirements of your CMS before you go searching online.
First, formulate your specific requirements, up front then compare them with the available packages offered by vendors. The following is how you can identify your user requirements.
• Each condition should be uniquely referenced not more than 250 words
• Prerequisite statements must not be copied or contradicted
• The user requirements specification express only requirements, not design
• Testable requirements
• Both parties understand user
• Elements should distinguish between desirable and regulatory features
• Need for requirement review between the customer and supplier
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