Quality Assurance in Laboratories
| Start Date | End Date | Venue | Fees (US $) | ||
|---|---|---|---|---|---|
| Quality Assurance in Laboratories | 19 Jul 2026 | 23 Jul 2026 | Riyadh, KSA | $ 3,900 | Register |
| Quality Assurance in Laboratories | 06 Sept 2026 | 10 Sept 2026 | Kuala Lumpur, Malaysia | $ 4,500 | Register |
| Quality Assurance in Laboratories | 29 Nov 2026 | 03 Dec 2026 | Dubai, UAE | $ 3,900 | Register |
Quality Assurance in Laboratories
| Start Date | End Date | Venue | Fees (US $) | |
|---|---|---|---|---|
| Quality Assurance in Laboratories | 19 Jul 2026 | 23 Jul 2026 | Riyadh, KSA | $ 3,900 |
| Quality Assurance in Laboratories | 06 Sept 2026 | 10 Sept 2026 | Kuala Lumpur, Malaysia | $ 4,500 |
| Quality Assurance in Laboratories | 29 Nov 2026 | 03 Dec 2026 | Dubai, UAE | $ 3,900 |
Introduction
Very often there are quality issues in the laboratory, which affect the standards that are intended and mean that quality can be in doubt for our clients. During various stages of processing we need to use quality tools to maintain confidence in the products. The analysis of each stage means that total confidence can also be achieved. This course is designed specifically for Laboratory technicians and those involved with quality control during the chemical process utilizing the most accurate tools and terms of measure for control. It contains full explanations in an easy to understand format and regular discussions to reinforce learning throughout.
Objectives
- Introduction to quality assurance in the laboratory and how principles of measurement are understood and utilized
- Principles of chemical measurement and the principles of quality assurance involved and used to their maximum
- Accurate measurement and recording of analysis and results of sampling of each step of chemical processes using quality tools
By the end of the training, participants will be able to
Training Methodology
This is an interactive course. There will be open question and answer sessions, regular group exercises and activities, videos, case studies, and presentations on best practice. Participants will have the opportunity to share with the facilitator and other participants on what works well and not so well for them, as well as work on issues from their own organizations. The online course is conducted online using MS-Teams/ClickMeeting.
Who Should Attend?
This course is intended for all Laboratory Supervisors, Technicians, and those involved with laboratory quality systems and controls.
Course Outline
Day 1: Introduction
- Philosophies
- Modern lab role
- Historical quality changes
Fundamentals of quality assurance (QA)
- QA=QA/QC, QA hierarchy, Costs/benefits of providing quality lab data and validation
- Budgeting and planning, QA location/function, Quality cycles, external/internal data validation
- The strategy of meeting user quality needs, specifications for QA leader
Day 2: Basic QA statistics: A brief overview
- Process merits, uncertainty types, comparing data, comparing labs, control charts (SPC)
- Systematic/random error, outliers/assignable cause/detection methods
- Lab vs field sampling error, accuracy/precision, Significant figures/reporting data
Measurement as a process
- Design/implement/monitor lab QA, macro/micro auditing, Internal and external lab auditing
- Screening and confirmatory analysis, Analyst certification, keeping staff current
- Development of QA programs
- Standards and reference materials, independent calibration verification
- Lab responsibilities, user responsibilities, Data handling/review/archiving/maintenance
- Lab certifications/accreditation
Day 3: Sampling
- General principles, criteria for developing sampling plans
- Sampling methods, fluids/solids, required information on samples
Sample handling
- Labeling, containers, filtering
- Preservation, holding times, conditions, transporting
- Blanks, chain-of-custody
Day 4: Sample preparation
- Procedures and protocols, reagent blank, miscellaneous topics
Instrumental analysis
- Instrument log, signal-to-noise ratio, instrumental parameters
- Calibration initial and continuing
- Causes and minimization of calibration drift
- Training of staff, cross-training
- Maintenance log, documentation, validation
Day 5: Standard operating procedures (SOP)
- Preparation recommendations, five W's, record keeping
- Changes to SOP, archives, distribution, OSHA and EPA compliance
- Glossary of terms and acronyms, safety-OSHA lab standard

