
January, 2013
CAPA Fundamentals Workshop, Developing CAPAs in the GCP Environment Conference
ExL Pharma
February, 2013
Audit-Readiness — Evaluating & Taking Steps to Ensure You Are Audit Ready Webinar
Society of Clinical Research Sites
February, 2013
Vendor Quality Oversight Webinar
DIA GCP SIAC
March, 2013
Reality vs. Perception — What a Site Really Needs To Do To Be GCP Compliant Webinar
Society of Clinical Research Sites
March, 2013
Advanced Clinical Vendor Oversight: Vendor Lifecycle Management
DIA Course
April, 2013
Successful Risk-Based Monitoring Implementation: Effective Strategies and Tactics for Your Organization
ACRP Global Conference
April, 2013
Successful Risk-Based Monitoring Implementation: Effective Strategies and Tactics for Your Organization
ACRP Global Conference
June, 2013
FDA Expectations in 2012: Investigator - Site
Health Care Compliance Association Research Conference
June,2013
Quality Oversight of CROs-Clinical Vendors
DIA Annual Meeting Tutorial
August, 2013
Risked Based Site Management Webinar
Society of Clinical Research Sites
December, 2013
Top 3 Audit Findings and Tips and Tools To Prevent Them Webinar
Society of Clinical Research Sites

"Liz's course provided fresh material and up-to-date with current FDA findings. The tools Liz provided were great to bring back to my company and she provides to course participants 'one hour free consulting' after her course - which I will take her up on! Liz was open on current issues, which is very valuable – maybe uncomfortable for some –but this needs to happen." Quality Oversight 101: Developing a Vendor Quality Management Plan Katie Driscoll-Alberta, Senior Director, Worldwide Quality Assurance, GCP & GPvP, Cephalon |