The need for digitalization in the pharmaceutical laboratories is continuously evolving & there is a need for a more unified approach to laboratory and data management.
Leading pharmaceutical and biotech companies are re-assessing the processes and digital tools (incl. information systems) they use to collect, handle and organize QC laboratories data. The proposed update of Annex 11 by EMA and PIC/S in November 2022 looks to include regulatory expectations for digital transformation.
This practical course provides an in-depth understanding of redesigning processes to automate & digitize them and brings clarifications on regulatory & business risks as well as the automation examples from Pharma laboratory environment. It will focus as well on effective computerised systems validation including IT infrastructure qualification & support. You will learn as well about the options to integrate the systems and maintain them, including upgrade of applications and change control.
Join us & enhance your digital laboratory automation journey to achieve greater innovation, collaboration & productivity.