Robert Gaertner, senior director of strategy for Veeva Vault Quality looks at the steps manufacturing companies need to take to improve their content management systems.
Ann Yellowlees founder of Quantics Biostatistics explores the importance of accuracy and precision in bioassays and how it can help boost manufacturing efficiency.
Peter Cusworth, account manager for industrial automation company Yokogawa explores the challenges pharmaceutical manufacturers in the UK are facing when it comes to data integrity.
John Norman, technical service representative for the Tooling and Tablets division at Natoli examines the importance of both dimensional and visual tool inspections and their direct relationship to final tablet quality.
Dr David Phillips, senior global product technology specialist , clean air at Thermo Fisher Scientific looks at how the adoption of advanced Class II BSCs in cGMP environments is helping to deliver safe and effective medicines.
Peter Zipfell, product marketing manager at Thermo Fisher Scientific explains how better software can help pharmaceutical manufacturers keep their data accurate.
William E. Weiser - senior director, Global Quality Systems, Pharma Services at Thermo Fisher Scientific explores the factors that make or break a successful compliant method transfer.
Beth Peckover, VP Global Delivery at Kallik, pinpoints the three areas businesses need to get right to ensure computerised systems used for labelling meet all GxP requirements set out by industry regulators.
Fernando Geijo and Xavier Ruiz, manager of QA for R&D and QRD auditor, respectively, at Azbil Telstar discuss the importance of adopting good practices in clinical research.
Mike Munnelly, marketing manager product inspection Life Sciences Manufacturing, Thermo Fisher Scientific explains why weighing is an essential part of quality control for pharmaceutical packages.
