Process & Data Governance
Workshops in Austin
Live Oak Workshops are designed to equip you with the knowledge and critical thinking strategies that lead to success in the advancement of your GXP career. As worldwide regulatory expectations in the world of data integrity and data governance change, our workshops prepare you with the skills necessary to interpret regulations, guidance, and regulatory action into simple approaches for managing your everyday GXP responsibilities with the efficiency needed to thrive.
Sign up now to join us as we discuss, debate, question, and tackle interesting regulatory case studies in the world of data integrity and data governance!
We offer our workshops in Austin, TX, and Dublin, Ireland; however, if you cannot travel and still want to join the fun, a hybrid link will be provided for those unable to attend in person. We utilize the newest “Owl Laboratories” technology to ensure our remote participants feel as immersed as possible. Contact Us for more details on joining our workshops via the hybrid link. We will try our absolute best to ensure your remote experience is as close to in-person as possible!
This workshop is designed to accommodate all experience/background levels. Whether you are a recent graduate or experienced professional, each Stage will challenge you to think critically through the lens of risk management. The more diverse our workshop, the better the outcome!
Interested in DISCOUNTS?
Contact Us at info@liveoakqa.com for larger groups and larger discounts!
Morning snack & Lunch included in the workshop! Join us for a complimentary happy hour Tuesday afternoon.
Discount hotel rates are available at the Hilton Garden Inn Austin University for early bird sign ups! Receive the link after you register.
OUR WORKSHOP MISSION
Stage 1 — Austin: Fundamentals of GXP Data Integrity/Governance
The Stage 1 workshop is focused on developing a solid understanding of the foundations of GXP data governance and data integrity assurance. In this two-day workshop we discuss current regulatory expectations and guidance, including the ALCOA principles, with the goal of developing a comprehensive understanding of how to operate efficiently within a GXP regulated environment. We discuss risk-based approaches to ensure regulatory compliance; referencing current regulations, regulatory actions, and harmonized guidance. Specific sub-topics include:
A modern interpretation of 21 CFR Part 11/EU Annex 11; including proposed updates to EU Annex 11 (2026)
FDA GMP regulation 21 CFR Part 211.68 – computerized systems in GMP
Guideline on computerised systems and electronic data in clinical trials (EMA, 2023)
PIC/s Final Guidance (June 2021): Data Integrity
Data Integrity expectations for GLP
Quality Risk Management & ICH Q9:
Design
Operation
Monitoring
Strategies for metadata (e.g. audit trail) review
Critical Thinking and Data Integrity
Each day will include hands-on case studies where participants will practice application of data integrity principles in real-life scenarios.
The Stage 1 workshop is designed for personnel engaged in regulated GXP activities (employees who create, review or approve GXP data), including employees who support GXP activities, such as IT professionals. This workshop moves beyond the ALCOA+ principles with a heavy emphasis on quality risk management and is relevant to both new and experienced employees as we discuss data integrity from a regulator’s perspective. This workshop is designed to set individuals up for success in an evolving regulatory environment that is rapidly adapting to new technologies.
Each topic is presented and discussed from a regulatory patient-focused perspective, with one objective being gaining the confidence necessary to address complicated questions (e.g., hybrid systems) during regulatory inspections and/or internal audits. When employees are able to confidently describe “why we do what we do” from a risk-based and patient-centric perspective, inspectors are better able to understand the site’s rationale, reducing misunderstandings and ultimately leading to improved regulatory/audit outcomes.
Who should join the Stage 1 Fundamentals course? Individuals working within a GXP environment that:
are required to operate efficiently within a regulated environment (QC, Manufacturing, Quality, Warehouse, Engineering, IT, etc.) where the integrity of data (paper or electronic) is considered critical to patient safety,
may (or are) tasked with contributing to investigations (e.g., deviations) that include data integrity concerns,
perform or participate in internal or external audits,
participate in computer system validation or IT systems management,
or field data integrity related questions (written or verbal) during regulatory or customer interaction.
