Validation Week celebrated it's 23rd annual meeting on October 17-19, 2017 with hundreds of delegates and nearly 120 different organizations. Below is a sample of the sessions included in the compendia, but for full session information click here.
Attendee acclaim:
"I gained the knowledge and literature necessary to bring back to my workplace to convince all departments that validation is a lifecycle and team effort." - Process Development Associate, Agillent
When you download this compendia, you have access to the hundreds of slides from the best and brightest in the industry, right at your fingertips!
Migration to Pharma 4.0 — Navigate Emerging Quality Compliance Challenges and Preview the Validation Road Ahead
Chinmoy Roy, Genentech Inc.
Explore the Parallels between Process Validation and Design Verification
Roberta Goode, MSBE, CQE, Goode Compliance International
FDA Inspection Readiness — Get Ready and Stay Ready to Assure Favorable Inspection Outcomes
Michael Barile, Barile & Associates, Inc.
Cybersecurity and Computer Systems Validation — What You Need to Know
Valarie King-Bailey, OnShore Technology Group, Inc.
Understand and Comply with FDA Requirements and Expectations
Karyn Campbell, FDA
Introduction to Statistics in Validation for the Non-Statistician
Alan Golden, MS, Abbott Molecular
Establish Effective Strategies for Managing the Validation Quality System
Paul L. Pluta, PhD, IVT Network, a division of UBM Americas; Associate Professor, Biopharmaceutics, University of Illinois at Chicago (UIC)
Maximize Audit Trail Technical and Business Review Procedures to Comply with Requirements
Ty Mew, Ofni Systems
Using Risk to Guide Implementation of Quality System Elements
Gamal Amer, PhD, Premier Compliance Services, Inc.
Design Sampling Plans that Align with Global Regulatory Expectations
Alan Golden, MS, Abbott Molecular
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