Webinar: A Practical and Standardized Approach to tackle Reagent Lot-to-Lot using CLSI’s EP26

Verification of reagent lot to lot is considered part of good laboratory practices and in many accreditation standards such procedures are required / mandated prior to the use of a new lot of reagent.

As with each new lot of reagent there is always a potential where quality control materials and/or patient sample performance may be impacted. There is a multitude of factors that can affect the performance of a new reagent lot which may include critical changes or updates in the reagent formulation from manufacturers, decreased stability of reagents either due to temperature excursions during transportation and storage or even handling errors to name a few.

This webinar is organized in collaboration with the Malaysian Association of Clinical Biochemists (MACB) in an effort to advance online education for medical professionals.


Date: 5 August 2021 | Thursday
Time: 2.30 pm - 3.30 pm Malaysia time
Location: Microsoft Teams

For a smoother webinar experience, please click on the link below to download the Microsoft Teams application to your computer or device that you will be using for this session.

Download Microsoft Teams

Mr Norizhar Bin Mohamed Zakaria

Clinical Quality Manager, Siemens Healthineers, ASEAN. Mr Izhar has over 16+ years of experience in Laboratory Management, Quality Assurance and Compliance, and Auditing (Reference/Vendor Labs). He is also a certified Inspector under the College of American Pathologists (CAP) Laboratory Accreditation Program.