Online Training 2016 - The Time is Nigh - An Actionable Timeline for IQCP Implementation - By Compliance Global Inc

Overview:
With only days left in 2015, the IQCP Transition and Education period ends on December 31, 2015! From January 1, 2014 ? January 1, 2016 there is an Education and Training Period for laboratories to learn about the Centers for Medicare and Medicaid Services (CMS) new Individualized Quality Control Plan (IQCP) Interpretive Guidelines, identify resources available and begin the implementation process.
Lab Directors across the country should be creating an Action Item Timeline for implementing IQCP if they are transitioning away from Equivalent Quality Control (EQC). The process for creating an IQCP should include time for learning about the requirements of IQCP prior to implementation. The goal of this webinar is to demonstrate an actionable timeline that is based on a daily interval so that laboratories can plan accordingly and set tangible deadlines for internal compliance.
Why Should You Attend:
Clinical Laboratory services who have performed Equivalent Quality Control for their laboratories must now either do IQCP transition or show justification that the manufacturer’s minimum QC requirement is acceptable for risk management and risk mitigation to reduce risk of harm to the patient.
Those laboratories who may have been performing the manufacturer’s minimum of two levels of QC per day of testing may see the value in transitioning to IQCP as a means to reduce risk of harm to the patient.
This webinar will explain who benefits from IQCP, what documentation is needed for compliance, and if a laboratory choses to only perform the manufacturer’s minimum of two levels of testing per day ? what supporting documentation may be helpful in ensuring regulatory compliance.
Areas Covered in this Webinar:
A realistic timeline for creating an IQCP before or after the January 1, 2016 deadline.
Identifying areas of risk mitigation for laboratory testing
Demonstrate an actionable timeline that is based on a daily interval so that laboratories can plan accordingly and set tangible deadlines for internal compliance
Learning Objectives:
Define the three components of IQCP (Risk Assessment, Quality Control Plan and Quality Assessment)
Identify key tasks that are crucial to the creation and implementation of the IQCP
Create an action based timeline for IQCP Implementation by the January 1, 2016 deadline
Who Will Benefit:
Physician Office Laboratories
Laboratory Directors
Laboratory Managers
Quality Assurance Departments
Risk Management Officers
Laboratory Accrediting Organizations
POCT Testing Groups
ASCP, AACC, AMT, ASCLS, CLSI, Advance, MLO, CLP, POR CMS, CAP, Joint Commission, COLA, A2LA, Accredited Laboratories
Speaker Profile:
Medical, Laboratory & Technology Consultants, LLC has extensive experience in working with partners in International and US governments as well as public and private sectors. Our consultants are experts in the medical and scientific fields who, given the opportunity to expand their knowledge base, became global players and local partners.
CEO, Professor Maria Stevens Hardy, IMA (ASCP), AHI (AMT) & CLC (AMT) is a third generation member of the Healthcare Workforce. After becoming a Quality Assurance Specialist at the age of 25 traveled to many developing and resource limited countries to improve challenges in healthcare systems. The one common challenge encountered was the implementation of Quality Management Systems and the execution of quality patient care initiatives.
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https://complianceglobal.us/product/700258
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