Meet our President
President & CEO
QD-Quality and Training Solutions, Inc.
Member, Board of Trustees
Association of Clinical Research Professionals (ACRP)
Call Us:
615.732.6035
Office hours: 8:30 am to 5 pm CST.
More Choices
Engagements 2013
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
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For a detailed course agenda, or to bring a course(s) to your organization (for a cost-effective 'flat fee per course'), please contact us. |
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These courses are provided on-site and provide attendees with the regulatory rationale for the activity as well as the specific job skill, in the classroom. For example, our Clinical Site Monitoring Course, an intensive course, provides case studies and scenarios/simulations for each type of monitoring visit, inclusive of investigational product accountability (pill bottles, accountability logs), subject case histories, case report forms, site regulatory binders etc.
Random Testimonial
"Liz provided thorough explanations to my questions with good practical examples." Good Clinical Practice for Medical Device IDE Trials Cheri Gee, Compliance Project Manager, Arthrocare |