Quality certificate ISO 9001 has been implemented in our company since 1999. Our Company uses standardized processes in production packaging with regard to the highest quality and the satisfaction of clients. The certification is under the regular audits from the part SGS, Czech Republic. Download HERE
We implemented within increasing quality services i.e. processing standardization. Processing standardization means printing production according to the valid international and profession printing rules as for example ISO 12647, Medien Standard Druck, Prozess Standard Offsetdruck etc. The aim of this process is to better stabilize the production - so it has also the positive effect on our clients in the increasing quality of printing products. It doesn´t involve only our internal process, but it takes just also customers in area pre-press data process. Detailed specified printing data is supposing for the standardized production process and expected and repeatable result. Except detailed printing data specification we can offer on our websites also easy instructions how to proceed in standard graphic programs generating printing PDF. Manual Print Quality, ICC profil, PDF X4 job options
Good Manufacturing Practise (GMP) presents in the pharmaceutical production system protection of consumer. It is complex of precautions that makes the minimum risk in order to not get the medicament of inconvenient quality or unsuitable for intended use. The printing company as the supplier of boxes for the pharmaceutical companies has to take a part of this strict system of rules and standards in order to not reach the market the medicament in inconvenient packaging or not happen exchanging the packaging or lots. For this reason we established in our company independent department quality control which task is to watch packaging quality not only for pharmaceutical industry. Quality department also surveys if also other strict standards of production practice are kept during all production process. We are able to meet our statement through the audit of the part pharmaceutical companies. Legislative data: The production medicaments has to be followed with requirements defined in law Nr. 378/2007 legal code., about medicaments and regulation Nr. 229/2008 legal code., about production and distribution of medicaments, that more detail specifies the requirements for production room , required controls, quality, staff etc. Law Nr. 79/1997, legal code amended by act Nr. 269/2003 legal code and later regulations. Directive: Committee 2003/94/EC, 2004/27/EC and 2004/28/EC, directive ICH Q7 (for EU, USA a Japan). Directions for the correct production practise are more detailed elaborated also here: Regulation of Ministry of Health 411/2004 legal code. Material EU - The Rules Governing Medicinal Products in the European Union, Volume 4, Good manufacturing practices (Czech translation- see Instruction SÚKL VYR-32, Bulletin SÚKL č. 2/2006).
Certification FSC® presents reliable certification system of consumer chain with the worldwide activity. Thanks its transparency, openness to all interest groups and thanks the strict social and ecological standard has FSC® support the biggest environmental organisations as WWF, Friends of the Earth or Greenpeace, just as the big retail chains as Hornbach, IKEA, B&Q or Home Depot. Through certification of manufacturing (consumer) chain (C-o-C, chain of custody) can be guaranteed that our packaging is made from the cardboard which contains a part of pure cellulose originated from the forests with certificate FSC®. In practise it means that every member in manufacturing chain from forest to customer has to obtain certificate FSC®. It makes the customer sure that he buys the product from carefully cultivated forests. Download HERE