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

Level

Intermediate

For registration:  https://www.complianceglobal.us/product/700258 

About Compliance Global Inc

Compliance Global Inc; is a training (webinar) organization based in New Hyde Park, New York, providing world-class compliance trainings and online webinars by leveraging a pool of experienced speakers / consultants in the Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance, Healthcare, BFSI, Life Science & HR streams for improving the knowledge base of the customers. Our trainings are contemporary, simple and cost-effective with easy access and great delivery experience. Compliance Global is a multifaceted entity, an absolute knowledge repository.

Our varied industry expertise ranges across Life Science (Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance), Healthcare, HR Compliance, BFSI, Food & Dietary Supplements, Insurance, Accounting & Taxation and other Cross Industry streams.

Email: referrals@complianceglobal.us

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