| The distribution of pharmaceutical products requires a great rigour at each stage of the supply chain, in order to guarantee the complete quality of the activity. The pharmaceutical industry also has to deal with counterfeit drugs, and has to respect European norms and standards.
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Drugs are not only perishable but require specific storage, for instance in order to control the temperature. So laboratories and distributors need a reliable system and a total traceability of logistic flows and events. To provide an adapted solution to our customers from pharmaceutical industry, a-SIS offers : - a tested methodology : rigourous roll-over and validation of each project step, the right definition of the team-project roles, regular meetings, and a detailed functional analysis
- a complete audit trail which enables you to trace and file all logistic operations, as well as the actions carried out by the operators on the system. This solution allows our customers to ensure their conformity to the GAMP and 21 CFR part 11 standards, regarding the quality of automated installations and the safety of systems and applications
- specific functions for the storage and the order preparation of the controlled temperature products
- complete traceability allows you to implement batch recall procedures and to reduce out-of-date problems
- tools which reinforce split box preparation quality: specific weight checking trolleys, or Voice_Picker® terminals which combine scans of batch numbers and voice guidance by the operators
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