
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


| Approach & Philosophy |
Our Philosophy is to provide short-term, focused services whereby our team will provide to you an infrastructure thnat you can maintain at the end of the project, without further need for on-going consulting services. We partner with you and your team to ensure success -- long after project completion.Our Approach is based on sound quality management principles, regulatory agency and industry driven requirements. |
"Liz is an excellent presenter and instructor. This course provided me with additional knowledge and skills to bring to my job." Quality Oversight 101: Developing a Vendor Quality Management Plan Sabrina Covic-Savic, The Medicines Company |