In the high­ly regu­la­ted health­ca­re sec­tor, com­pa­nies must con­ti­nuous­ly adapt their pro­ducts to the gro­wing cus­to­mer requi­re­ments within the frame­work of legal requi­re­ments and spe­ci­fi­ca­ti­ons, e.g. from the EMA, FDA and GMP. In the sales pro­cess of the usual­ly high­ly com­plex pro­ducts, clear pri­cing and cor­rect quo­ta­ti­on pre­pa­ra­ti­on is enorm­ously important, which often turns out to be chal­len­ging.

CPQ con­fi­gu­ra­ti­on soft­ware such as CREALIS® sim­pli­fies the sales pro­cess for manu­fac­tu­r­ers of mul­ti-vari­ant pro­ducts. The soft­ware enables the cor­rect orga­ni­sa­ti­on of fea­tures and com­pon­ents of com­plex pro­ducts, taking into account depen­den­ci­es and coun­try-spe­ci­fic requi­re­ments. In this way, accu­ra­te, indi­vi­du­al quo­ta­ti­ons are crea­ted within a short peri­od of time.

In the Euro­pean mar­ket, CE cer­ti­fi­ca­ti­on is essen­ti­al for the dis­tri­bu­ti­on of medi­cal pro­ducts. This requi­res exten­si­ve, detail­ed tech­ni­cal docu­men­ta­ti­on that can be shown in the CPQ soft­ware along with the asso­cia­ted docu­ments and cer­ti­fi­ca­ti­ons.

With the CREALIS® CPQ con­fi­gu­ra­ti­on solu­ti­on, medi­cal tech­no­lo­gy com­pa­nies are thus well pre­pared for the con­stant­ly incre­asing cus­to­mer and mar­ket requi­re­ments in their indus­try.

CPQ-Lösungen_Medizintechnik