Free Webinar Alert!

Published on 03/16/2023 11:20 AM by: newsuser Category: None

To all DOST OneLab Member Laboratories:

You might be interested to participate in this free webinar to be organized by the Standards and Testing Division (STD) of DOST-ITDI:

Topic: FREE Webinar on the Preparation of Internal Quality Control Material (IQCM) based on ISO Guide 80

Date: 30 March 2023

Time: 09:00 AM - 04:00 PM Philippine Standard Time (01:00 AM - 08:00 AM UTC)

Cost: FREE of Charge

For Registered Chemists and Registered Chemical Technicians in the Philippines, this webinar has been granted 5.00 CPD units by the Professional Regulation Commission (PRC) Continuing Professional Development (CPD) Council for Chemistry.

This Free Webinar is brought to you by the Standards and Testing Division (STD) of the Industrial Technology Development Institute (ITDI), Department of Science and Technology (DOST), Philippines. Presentations in this webinar are from the analytical data from the completed GAA-funded research and development projects of the Division for 2022. Only maximum of 300 participants will be accommodated.

For DOST OneLab Network member laboratories, a maximum of three (3) participants are allowed to register. For non-member laboratories/organizations, a maximum of two (2) participants are allowed. Limited slots are given per laboratory/organization in order to accommodate as much laboratories/organizations as possible. Registration will be screened and accommodation is on a first-come-first-served basis. PRIORITY is given to DOST OneLab Network member laboratories.

Webinar Description:

The purpose of this webinar to provide participants with the knowledge in the preparation and characterization of an Internal Quality Control Material (IQCM) based on ISO Guide 80:2014 "Guidance for the in-house preparation of quality control materials (QCMs)."

Webinar Takeaways:

Upon completion of the webinar, the participants will be able to learn the following:

1. Identification of a suitable candidate material to be used as internal quality control material (IQCM);

2. Assess the suitability of the validated test method to the candidate material;

3. Processing and bottling of the candidate material for homogenization, sub-division and packaging;

4. Conduct of homogeneity assessment to determine if the candidate IQCM developed is adequate and sufficiently homogenous;

5. Characterize the developed IQCM using validated/verified test method;

6. Evaluate stability over a period of time ; and

7. Incorporate the developed IQCM into the laboratory’s internal quality control program.

Please let us know if you have questions/clarifications on this activity. We do hope you can join us.