23rd Annual Validation Week Compendia

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