
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


| Pharmacovigilance Training Course |
This course is provided on-site in alignment with company policies, SOPs and standards for adverse event and product quality complaint reporting.
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"Liz has great background in many areas of research, enabling her to use concrete examples in her training. She uses multiple teaching techniques to keep the audience involved and enthused. She also provided excellent materials, and has a light-hearted, energetic manner." Good Clinical Practice for Medical Device IDE Trials Pam Aakhus, Patient Recruitment Specialist, Arthocare |