Our guarantees in the most demanding sector
The regulatory framework in the pharmaceutical industry is necessarily one of the most stringent. To comply with CFR 21 part 11 or EU GMP Annex 11, and others, highly specialised digitalisation expertise on platform processes and MES, MOM, EBR, BMS, EMS, OEE, IPC, and QMS is essential.
Our team is highly qualified, possessing both the training and specialist expertise to design and implement these types of solutions. We can provide you with everything from electric panels and installations to the software itself for both GMP and non GMP environments. And as we know that development is just as important as ongoing support, we are on hand for assistance through our 24/7 support service.