Quality & Productivity

ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting – London, 29 Mar – 2 Apr 2027

ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting runs in London from Monday 29 March to Friday 2 April 2027 (1 Week). The fee is 23,000 SAR per participant. The same programme is also scheduled in 7 other cities.

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Dates
Length
1 Week
Fee per participant
23,000 SAR
Format
In person, London
Venue
Central London four-star
Status
Open for registration
Week
13 of 2027
Reference
351_12978

This session

29 Mar – 2 Apr 2027

This ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting session in London runs from Monday 29 March to Friday 2 April 2027 (week 13, Q1 2027). It is the 1st of 2 dates in London in 2027, at a fee of 23,000 SAR, the same for each of them. Registration is open for this date. It is held in person at Central London four-star.

When else does it run in London?

How do I book this date?

Register online to request your place, or send us a question about this date first.

Reference for this date: 351_12978. Quote it when you contact us.

Before you book, read our cancellation policy.

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Questions about this date

When does ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting in London start and finish?

It starts on Monday 29 March and finishes on Friday 2 April 2027: 1 Week.

How much does ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting in London cost?

The fee for this date is 23,000 SAR per participant. Please read our cancellation policy before you book.

Is this date held in person or online?

It is held in person in London, at Central London four-star.

Where else does ISO 15189 Medical Laboratory Quality: Specimen Control, QC and Result Reporting run?

It is also scheduled in 7 other cities: Amsterdam, Barcelona, Dammam, Dubai, Jeddah, Paris and Riyadh.

What does this programme cover?

ISO 15189 medical laboratory quality depends on every patient specimen being collected, identified, analysed and reported without error, yet most laboratory mistakes arise before or after the analyser, in mislabelled tubes, unnoticed control shifts and critical values that never reach the clinician. This Core Concept course equips clinical laboratory staff to control the total testing process against ISO 15189 requirements: specimen acceptance, internal quality control with Westgard rules, external quality assessment, method verification, critical result notification, turnaround time, LIS traceability and biosafety. Participants produce a Medical Laboratory Total Testing Process Control Plan.

The programme outline covers:

  • Introduction
  • Course Objectives
  • Target Audience
  • Course Outline
  • Day 1: The Clinical Laboratory Total Testing Process and ISO 15189
  • Day 2: Pre-Analytical Control: Specimen Collection, Labelling and Acceptance
  • Day 3: Analytical Quality: Internal QC, EQA and Method Verification
  • Day 4: Post-Analytical Risk: Critical Results, TAT, LIS and Biosafety
  • Day 5: Case Study Workshop: Accreditation Readiness and the Control Plan
  • Skills You Will Gain
  • Why Attend This Course
  • Conclusion
Read the full outline on the programme page ↗

Where else does this programme run?

Also scheduled in 7 other cities.

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