Quality in the Life Science Industries is no longer an optional exercise it is now obligatory. After many scandals this was demanded by end consumers and then made compulsory by legislators so that a meticulous quality audit trail is now one of the main success factors. Whether in the manufacture of medicines or foods – the implemented software for quality management is also a critical success factor for all sectors of the Life Science Industries. It does not matter how much care is taken towards quality orientation, it means nothing if the implemented system does not actively support and follow the statutory frameworks that have been laid down.
This is where the GUS solutions show their strength. Their flexible applications are continually adapted to the actual demands in the market and they react to new legislations with function extensions. For more than 28 years the GUS Group has supported the sectors pharmaceuticals, food, biotechnology, cosmetics and chemicals and is fully aware of the particularities of these industries. The GUS Group has been following current regulations such as the General Good Law, validation or 21 CFR Part 11 for a long time. Furthermore for many years now the GUS Group has oriented itself on the standard WHO principles – Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Storage Practice (GSP) and the statutory drug laws. GUS-OS ERP is an ERP system that features comprehensive quality management which allows meticulous lot tracing.
The GUS Group has not only set the target to improve the quality management of its customers, they are themselves fully committed to quality: the whole organization is ISO 9001:2008 certificated and they regularly tale part in supplier audits.
>> The Quality-Charta of the GUS Group
>> Quality-Management System
>> ISO 9001:2008-Certificate (download)
