EPM speaks to Abdullah Al-Hakimi, senior quality compliance specialist at Autolus and Robert Gaertner, strategy director for Veeva Vault Quality, about working during Covid-19 and why quality processes are so important in pharma.
Vanessa Fachada Oliveira, pharmacovigilance manager & EU QPPV at Arriello, highlights key areas of focus for marketing authorisation holders to achieve an effective audit of their pharmacovigilance systems.
Andreas Gross - global product manager of Inspection Technology at Syntegon Technology, explains how artificial intelligence (AI) is being used to ensure pharmaceutical products are safe.
Bart Vansteenkiste, life science sector manager, Domino Printing Sciences, outlines how pharmaceutical companies can improve validation processes to improve their overall compliance.
Patrick Kenny, product marketing specialist for Thermo Fisher Scientific explains why the storage and access of chromatography data is vital to pharmaceutical manufacturing chains.
Robert Gaertner, director of strategy for quality at Veeva, explains how digital transformation is improving pharmaceutical processes across the industry.
Gero Lustig, global business manager Pharma and Life Sciences at ABB explains how using a digital twin of existing machines can determine how best to implement shop floor integration prior to installation.
Zak Yusoff, pharmaceutical freeze-drying applications manager at SP Scientific discusses why a quality by design (QbD) approach is key to achieving optimal lyophilisation of limited and expensive biopharmaceutical drugs.
