
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


| On-Site Training |
Our standard repertoire of courses can be brought to your site, whether you are a sponsor company, investgational site, academic institution, CRO or professional organization. We have delivered these as customized courses for both our sponsor client companies and investigational site personnel to address targeted training needs for these organizations. This is a very cost effective solution for your budget, as we charge one fee for each day of training.
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"Liz has tremendous depth of knowledge in the field, a great resource and it is great to discuss issues with her. I will implement specific strategies discussed in the course in my job." Current Landscape of FDA Expectations: Sponsors & Investigators Deb Chapman, Clinical Operations, Portola Pharmaceuticals |