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The system adheres to ISO9001 as well as manufacturing
standards as set out by The Irish Medicines Board and GMP |
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The system supports the concept of an isolation or quarantine
area, where non-conforming, materials, packaging and finished
product can be held, awaiting approval. |
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Facility to hold details of finished product specifications
for reference |
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Facility to query and analyse customer complaints in a
user-friendly easily accessible format |
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Facility to trace complaints on products back to all stages of
production. |
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The ability to produce QC labels displaying quality data at
various stages of the production process.
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