News & Events
Technical diagnostics updates, ISO standard training schedules, and medical laboratory science thought leadership.
Risk Management Training for Medical Laboratories (ISO 22367:2020)
Keton Consulting is proud to announce its upcoming specialized training on Risk Management for Medical Laboratories according to the ISO 22367:2020 standards. This intensive session is tailored for laboratory managers, quality officers, and pathologists seeking to enhance safety and compliance. Participants will learn practical methodologies for identifying, assessing, and mitigating risks within a clinical laboratory environment. ISO 22367:2020 provides specific requirements to control risks associated with medical laboratory examinations, and Keton offers hands-on guidance from certified lead auditors and technical experts. Sign up today using our official enrollment channel.
Advancing Laboratory Medicine: SNIBE Biossays Integration in East Africa
Clinical diagnostics is undergoing a massive shift towards automation. Keton Consulting is spearheading this evolution by deploying high-throughput SNIBE Biossays analyzers across multiple healthcare facilities in East Africa. These platforms deliver exceptional accuracy and minimize analytical error rates, significantly improving time-to-result. Our deployment package includes complete setup, KEBS verification, and 24/7 technical backup to ensure clinical testing runs uninterrupted. Discover how integrating advanced chemistry diagnostics can optimize operations and deliver superior patient outcomes.
Understanding EQA: Why Method Verification and Quality Controls Matter
External Quality Assurance (EQA) is a key pillar of medical laboratory accreditation and trust. This article explores the core steps of method verification, proficiency testing, and the critical role of third-party control materials in ensuring daily testing reliability. Keton Consulting offers complete EQA programs in partnership with ESfEQA and audit microcontrols, helping laboratories identify system inaccuracies, perform effective Root Cause Analysis (RCA), and maintain 100% regulatory compliance. Learn the structured pathway to standardizing your quality metrics.