The Paperless Lab Academy is owned and organized by NL42 Consulting, industry domain experts and independent advisors operating from Europe with consultancy practices throughout the globe.
The Paperless Lab Academy project initiated in 2013 with a strong focus on creating the ideal learning platform for those considering consolidating, integrating and simplifying scientific data management systems.
[PRESS RELEASE] PLA Announces new management yet same objectives at the #PLA2017
Eric De Maesschalck
Eric graduated in Clinical Chemistry and Medical Biology. He has spent 32 years in highly regulated biopharmaceutical companies: GSK, Pfizer, Phibro Animal Health and UCB BioPharma. Eric has 27 years of experience in computerized systems qualification and validation including IT infrastructure (GMP, GCP, GLP, GPvP)
Eric is currently heading the Corporate QC Laboratory Digitalization position at UCB Pharma, where he manages a team dealing with laboratory equipments (Data capture, Data integrity), and is also in charge of ensuring the correct and smooth integration and transition of the computerized systems processes, from analytical development laboratories to commercial quality control laboratories implemented across UCB sites. Eric is therefore involved in global and transversal initiatives like Knowledge management, technical landscape redesign, data capture governance definition, Enterprise 4.0 and UCB Technical & Supply Organization digital projects.
Mark is an independent consultant in laboratory informatics and data, data integrity, validation of computer systems/spreadsheets, analytical instruments and LIMS/ELN. He has 30+ years of pharmaceutical experience in QC Labs, computer systems validation and lab informatics at Eli Lilly
Mark co-lead Eli Lilly’s data integrity remediation program for QC Labs worldwide in 2012, consulted and audited several Lilly sites preparing for data-integrity focused inspections.
He is a co-leader for the GAMP Data Integrity Special Interest Group and Chair of ISPE Global Documents Committee.
Co-author of "Harmonizing USP <1058> and GAMP for Analytical Instrument Qualification" Schuessler, Newton, Smith, Burgess, McDowall. Pharm. Engineering, Jan/Feb 2014
Co-editor of the GAMP Good Practice Guide "A Risk-Based Approach to Compliant Computerized Laboratory Systems" Nov. 2012.
Chemist from the University of Barcelona, May is working at Dow Chemical Iberica in Tarragona for more than 20 years.
She started in R&D Plastics, working on different development projects (at-line; on-line; off line type of instruments) which have required transfers to the Netherlands and to Germany.
She then expanded to TS&D support type of projects, with specific analytical needs or methodologies to be implemented or developed. Afterwhat, she moved to the Manufacturing Department leading the 3 onsite Labs. Nowadays she´s statistical manager in the Data Services department providing support to their internal customers (plants, labs ...) for a better use of their data and delivering talks on how they address the Industry 4.0 and the Big Data concepts at Dow.
Sofie van der Meulen
Sofie works for the Dutch Data Protection Authority. In her position as senior supervision officer she focuses on privacy in the healthcare sector.
Before joining the Dutch Data Protection Authority, Sofie has gained broad experience dealing with various kinds of legal issues in both profit and non-profit environments.
In her previous position as attorney at law in the field of life sciences, Sofie specialized in legal and regulatory issues related to medicinal products and medical devices, with a special focus on medical software, big data and data protection.
Bridging the worlds of R&D and IT for global programmes that transform the way science is done in Unilever R&D, like enabling eScience. Key topics were introducing the use of an ELN to capture exploratory research, creating a repository of scientific data for modelling, and computer simulations of products.
Mr. Pijanowski brings over 30 years of professional experience related to laboratory operations and scientific informatics.
Throughout that time, Pat has served in various roles focusing upon LIMS, Electronic Laboratory Notebooks, laboratory instrumentation and related scientific data systems.
During the past 6 years, he has managed a Pharmaceuticals & Life Sciences consulting practice within LabAnswer, and delivered strategic advisory services to many of the world’s top life sciences organizations. Prior to joining LabAnswer, Pat served as the Chief Operating Officer for LabVantage Solutions, and prior to joining LabVantage, he served as the General Manager of the LIMS business unit within Applied Biosystems.
Pat is today the Managing Director at Accenture Scientific Informatics Services after the acquisition of labAnswer by Accenture