Course description
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 regulated laboratories. It will focus as well on effective computerised systems validation including leveraging supplier development and testing to reduce your overall effort. 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.
