CLIA Compliance - From Quality Control to Inspections - Comprehensive Training Package (3 Courses)

Instructor: Barry Craig
Product ID: 702293
This comprehensive training package of three courses is aimed at helping clinical laboratories ensure compliance with CLIA requirements.

Training CD / USB Drive

$1,499.00 (66%)
Save $1,000.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

The Clinical Laboratory Improvement Amendment (CLIA) regulatory requirements can be difficult to understand and follow. Are you sure your laboratory is in compliance with the various requirements?

To help clinical laboratories ensure regulatory compliance, we have created this package of 3 CLIA webinar recording CDs covering topics such as CLIA guidelines on quality control; calibration, calibration verification and method validation; and how to prepare for, and handle, the CLIA laboratory inspection.

How It Works:

Each webinar CD has a series of modules. Our speakers have delivered the modules using PowerPoint slides.

This training is convenient to attend individually or in groups. You don’t have to travel from your office. This means you can afford to have your whole team attend. As the webinar recording CDs are licensed to be used multiple times in a location, you can schedule the training as many times for as many groups/batches as you wish. Your team members will learn the material together; everybody will get the same information.

Webinar Topics:

Who will benefit?

These webinar recording CDs will be beneficial to the following:

Clinical Lab personnel; the Physician Office Lab personnel; Reference Lab personnel; Lab Directors; Quality Assurance Managers and auditors; Laboratory Personnel; Laboratory Supervisors; Nurses, Medical Assistants, or anyone filling a laboratory role; Instrumentation specialist; and Medical supply reps.

Webinars included in the Package:

CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment (Duration: 60 minutes)

This Clinical Laboratory Improvement Amendments (CLIA) training is aimed at CLIA regulated non-waived laboratories that run automated analyzers or semi-quantitative kit tests.

Areas Covered in the Webinar:

  • Quality Assurance vs. Quality Assessment: Why the Change?
  • The Three Phases of Testing.
  • Quality Assessment Systems That Work.
  • Quality Control: Principles and Practice.
  • QC for Waived Testing: Is Minimum Enough?
  • QC Formulas and Their Use.
  • Why QC and QA are linked processes.
  • Measurement indicators for QA.

Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations: Calibration, Calibration Verification and Method Validation (60 minutes)

The Clinical Laboratory Improvement Amendments (CLIA) training outlines the CLIA standards for frequency, methodology and also give examples of practical application.

Areas Covered in the Webinar:

  • What do calibration, calibration verification and method validation mean?
  • When each of these processes should take place.
  • What systems are required to use these processes and which ones are not.
  • Requirements for validation of new test systems.
  • Remedial action if these processes are unsuccessful or have unexpected results.
  • Reasoning behind each process and why they are necessary.

The CLIA Laboratory Inspection: Failure is not an Option (60 minutes)

This CLIA Laboratory Inspection training will discuss the salient features of laboratory inspection as per CLIA inspection guidelines.

Areas Covered in the Webinar:

  • Preparation is the Key.
  • The Laboratory Walk-Thru.
  • Personnel Training/Competency Documentation.
  • Quality Control: The Core of the Inspection Process.
  • Quality Assessment Plan: What Do You Measure?
  • Patient Chart/EMR Review.
  • Inspection Follow-up and Response.
  • General Guidelines for a Successful Inspection.
  • CLIA vs other accreditation inspections.
  • Post survey considerations.

About the Instructor:

Barry Craig , Owner and CEO of Laboratory Consulting, LLC, has over 20 years of experience in laboratory management with a concentration on physician office labs. He managed 22 COLA accredited POL's, half waived, half non-waived. He has been published in ADVANCE for Administrators of the Laboratory magazine. He teaches a seminar on Lab Consulting at the annual COLA symposium.

Follow us :
Biostatistics for the Non-Statistician
Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed