Pharmaceutical companies are extremely sensitive with regard to how documents & records are managed and accessed. It is not only vital to optimise efficiency but to manage these records from a regulatory perspective.

Stringent regulations such as the FDA 21 Part 11 have made compliance managers take a serious look at their document review practices. Partnering with ABBYY and ZyLAB both global leaders in their field of expertise, Informa have the technology available to provide solutions that are the best in their field but also conform to regulatory requirements for this industry.