Digitalisation solutions for pharmaceutical environments (GMP / Non GMP)
If there is one sector that operates extremely high-quality standards, it is the pharmaceutical sector.
It is one of the leading industries for R+D with 19% of the total investment made in the country. It generates more than €15bn per year and is also the driving force behind almost 25% of the high technology produced. The traditional challenges are joined by new demands in computer system digitalisation and validation that must comply with increasingly strict regulations.
That’s why we provide reliable innovative production management and control solutions to a sector that works to look after our health and drive us forward.
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.