Are your lab results raising red flags? Know what matters clinically — and what doesn’t.
When IQC and EQA results fall outside acceptable limits, it’s no longer just about technical nonconformities — it’s about potential clinical harm. ISO 15189:2022 (Clauses 7.3.7.2 g and 7.3.7.3 h & i) requires medical laboratories to determine whether these failures may have affected patient results. Yet, many labs either skip this step or lack a clear process to assess clinical significance.
This high-impact webinar is designed to close that gap. You’ll learn how to move beyond routine reporting to critically evaluate the patient impact of IQC and EQA failures — and most importantly, how to manage and prevent such errors. If you’re committed to quality, accreditation, and above all, patient safety, this is a session you can’t afford to miss.
📅 Date: 𝟐𝟑𝐫𝐝 𝐌𝐚𝐲 𝟐𝟎𝟐𝟓
⏰ 𝐓𝐢𝐦𝐞 𝐙𝐨𝐧𝐞𝐬
🇰🇪 Kenya (EAT): 3:30 PM – 5:00 PM
🇿🇦 South Africa (SAST): 2:30 PM – 4:00 PM
🌍 GMT: 12:30 PM – 2:00 PM
𝐄𝐚𝐫𝐧 𝟑 𝐂𝐏𝐃 𝐏𝐨𝐢𝐧𝐭𝐬
💰 𝐂𝐏𝐃 𝐏𝐫𝐨𝐜𝐞𝐬𝐬𝐢𝐧𝐠 𝐅𝐞𝐞: 𝐊𝐄𝐒 𝟏𝟎𝟎 only
𝐏𝐚𝐲𝐛𝐢𝐥𝐥 𝐍𝐮𝐦𝐛𝐞𝐫: 400222
𝐀𝐜𝐜𝐨𝐮𝐧𝐭 𝐍𝐮𝐦𝐛𝐞𝐫: 1083331#YOUR NAME
📍 𝐑𝐞𝐠𝐢𝐬𝐭𝐞𝐫 𝐍𝐨𝐰:
https://lnkd.in/dTMtrnbD
✨ 𝐄𝐥𝐞𝐯𝐚𝐭𝐞 𝐲𝐨𝐮𝐫 𝐥𝐚𝐛’𝐬 𝐫𝐞𝐬𝐩𝐨𝐧𝐬𝐞 𝐭𝐨 𝐈𝐐𝐂 & 𝐄𝐐𝐀 𝐟𝐚𝐢𝐥𝐮𝐫𝐞𝐬.
𝐑𝐞𝐠𝐢𝐬𝐭𝐞𝐫 𝐭𝐨𝐝𝐚𝐲 — 𝐬𝐩𝐚𝐜𝐞𝐬 𝐚𝐫𝐞 𝐟𝐢𝐥𝐥𝐢𝐧𝐠 𝐟𝐚𝐬𝐭!
