
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


| Quality Systems for Clinical Development Departments |
Analysis of clinical quality systems infrastructure and recommendations to support efficient and effective business processes as well as regulatory agency inspection readiness.
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"This course was extremely helpful. I have experience with a joint FDA and EMA inspection and Clinical Oversight was a critical factor with the CRO. Liz is knowledgeable on this topic and provided good examples in the course. The course handouts were very good and will be useful to take back to my company and use to discuss with the clinical group." Quality Oversight 101: Developing a Vendor Quality Management Plan Ron Lang, Senior Director, Quality Assurance, Valeant Pharmaceuticals |