Manufacturing, Engineering and Technology Fabrication and Extraction

Hplc Analysis And Quantification Of Prepared Samples Training

SAQA US 110388 | NQF 4 | Credits 13 | Duration 10 Days
From $1,933 per delegate

Description

This course equips learners with the skills to perform high-performance liquid chromatography (HPLC) analysis and quantification of prepared samples in a laboratory setting. Participants will gain practical competence in operating HPLC equipment, interpreting chromatograms, and ensuring accurate quantification of analytes. The training is aligned with SAQA unit standard 110388 and is designed to meet industry requirements for quality assurance and regulatory compliance.

Learning Outcomes

  • Apply HPLC principles and instrumentation to prepare and analyze samples according to standard operating procedures.
  • Demonstrate correct calibration and operation of HPLC systems, including pump, injector, column, and detector components.
  • Analyze chromatographic data to identify and quantify target analytes using appropriate software and calculations.
  • Evaluate the quality of HPLC results by performing system suitability tests and troubleshooting common issues.
  • Implement safety and quality assurance protocols in the HPLC laboratory to ensure reliable and reproducible outcomes.
  • Document analytical results and maintain records in compliance with laboratory standards and regulatory requirements.

Target Audience

This course is intended for laboratory technicians, analysts, and quality control personnel who are involved in HPLC analysis and require formal recognition of their competencies. It is also suitable for individuals seeking to upskill in chromatographic techniques within pharmaceutical, chemical, food, or environmental testing laboratories.

Prerequisites

None — open enrollment.

Course Outline

Day 1: Introduction to HPLC and Quality Assurance

Objectives:
• Understand the principles and components of HPLC
• Explain the role of quality assurance in HPLC analysis
• Identify safety protocols in the laboratory
• Describe the importance of sample preparation

Topics:
• Overview of HPLC: history, applications, and advantages
• Key components: pump, injector, column, detector, data system
• Quality assurance principles: ISO 17025, GLP
• Laboratory safety and waste management
• Introduction to sample preparation techniques

Day 2: The HPLC Instrument and Its Operation

Objectives:
• Identify and describe each module of an HPLC system
• Understand the function of mobile phases and solvents
• Perform basic instrument start-up and shutdown
• Recognize common instrument issues and troubleshooting

Topics:
• Detailed anatomy of HPLC modules
• Mobile phase selection and degassing
• Isocratic vs. gradient elution
• Instrument start-up, equilibration, and shutdown procedures
• Routine maintenance and troubleshooting

Day 3: Chromatography Theory and Separation Mechanisms

Objectives:
• Explain retention, selectivity, and efficiency
• Differentiate between normal-phase and reversed-phase chromatography
• Understand the role of column chemistry
• Calculate resolution and theoretical plates

Topics:
• Retention factor and selectivity
• Van Deemter equation and efficiency
• Normal-phase vs. reversed-phase HPLC
• Column selection: particle size, pore size, bonding
• Resolution calculation and optimization

Day 4: Sample Preparation Techniques

Objectives:
• Apply proper sample preparation methods
• Perform filtration, dilution, and extraction
• Understand the importance of sample integrity
• Prepare calibration standards and quality control samples

Topics:
• Sample filtration and centrifugation
• Liquid-liquid extraction and solid-phase extraction
• Derivatization techniques
• Preparation of calibration standards and QC samples
• Sample storage and stability

Day 5: Method Development and Optimization

Objectives:
• Develop a basic HPLC method for a given analyte
• Optimize mobile phase composition and flow rate
• Select appropriate detector wavelength
• Validate method parameters

Topics:
• Steps in method development
• Mobile phase pH and buffer selection
• Gradient optimization
• Detector selection: UV-Vis, fluorescence, RI
• Method validation parameters: specificity, linearity, precision

Day 6: Quantification and Calibration

Objectives:
• Understand external standard and internal standard methods
• Create calibration curves and evaluate linearity
• Calculate concentration of unknowns
• Apply statistical concepts to quantification

Topics:
• External standard calibration
• Internal standard calibration
• Calibration curve construction and linear regression
• Limit of detection and limit of quantification
• Statistical evaluation: R², residual analysis

Day 7: Data Analysis and Interpretation

Objectives:
• Interpret chromatograms and identify peaks
• Integrate peaks and correct for baseline drift
• Use software for data processing
• Report results in a standardized format

Topics:
• Chromatogram interpretation: peak identification
• Integration parameters: slope sensitivity, width
• Baseline correction techniques
• Data processing software functions
• Report generation and documentation

Day 8: Troubleshooting and System Suitability Testing

Objectives:
• Identify common HPLC problems and their causes
• Perform system suitability tests (SST)
• Interpret SST results and take corrective actions
• Maintain instrument performance

Topics:
• Common issues: pressure fluctuations, baseline noise, peak tailing
• System suitability parameters: retention time, resolution, tailing factor
• SST acceptance criteria
• Preventative maintenance schedule
• Documentation of troubleshooting

Day 9: Advanced Applications and Regulatory Compliance

Objectives:
• Explore advanced HPLC modes (e.g., UHPLC, chiral)
• Understand regulatory requirements for pharmaceutical analysis
• Apply HPLC in food, environmental, and clinical labs
• Prepare for audits and inspections

Topics:
• UHPLC and fast separations
• Chiral chromatography
• Regulatory guidelines: USP, ICH, FDA
• Application in pharmaceutical analysis
• Audit preparation and documentation

Day 10: Practical Integration and Assessment

Objectives:
• Integrate all skills into a complete analysis workflow
• Perform a full HPLC analysis from sample to report
• Complete a practical assessment
• Review and reflect on learning outcomes

Topics:
• Full workflow: sample prep, method setup, calibration, analysis, data processing
• Practical assessment: unknown sample quantification
• Review of key concepts
• Feedback and certification process

Practicals

32 hours of practicals To be conducted online or on-campus or in-house
Overview

Hands-on practical sessions are essential for learners to gain proficiency in HPLC operation, sample preparation, method development, and data analysis. These sessions allow learners to apply theoretical knowledge in a controlled laboratory environment, ensuring they can independently perform HPLC analysis and quantification.

Practical Activities
  • HPLC Instrument Familiarization and Operation — Learners will identify HPLC modules, perform start-up and shutdown, set up a simple isocratic method, and inject standards. (8h)
  • Sample Preparation and Calibration — Learners will prepare samples using filtration and dilution, create calibration standards, and construct calibration curves. (8h)
  • Method Development and Optimization — Learners will develop a simple reversed-phase method, optimize mobile phase composition and flow rate, and perform system suitability tests. (8h)
  • Full Analysis Workflow and Assessment — Learners will complete a full analysis from sample preparation to final report, including troubleshooting and data interpretation. (8h)

Summatives

Each delegate is assessed continuously throughout the course via daily exercises, scored practical assignments, and a final summative test at the end.

Practical Assignments — 30%

Practical assignments are observed and scored against a rubric during the practical sessions. Each delegate's practical mark is averaged into a single 100% score and contributes 30% to the final total.

Daily Exercises — 20%

Every training day ends with a multiple-choice exercise scored out of 100%. The scores from each daily exercise are averaged across the duration of the course to produce a Daily Average mark, which contributes 20% to the final total.

Final Test — 50%

On the last day a final summative test is written. It is a multiple-choice paper with multiple-answer questions: each question may have more than one correct option, and a single wrong selection on a question marks the entire question wrong — no partial credit. The final test is scored out of 100% and contributes 50% to the overall mark.

Final Total
Component Out of Weight
Practical Assignments (rubric-scored) 100% 30%
Daily Average (multiple choice) 100% 20%
Final Test (multi-answer multiple choice) 100% 50%
Final Total 100%

All marks are recorded on the AATICD LMS and visible to each learner under their account.

Certificate

Certificate of Completion

Awarded to delegates who achieve an overall mark of 50% or higher on the Final Total (Practicals 30% + Daily Average 20% + Final Test 50%).

How it works
  • Certificates are auto-generated on the AATICD LMS as soon as the marks pass the 50% threshold.
  • Each certificate is a branded PDF with the delegate's name, the course title, the unit standard ID, NQF level, credits, and the date of issue.
  • You can download or print your certificate from your LMS dashboard at any time after issue — there's no reissue fee and no expiry date.
  • If you scored under 50% you can sit the final test again at the next scheduled session at no extra cost.
Where to find it

Sign in to the LMS, open your dashboard, and your certificates appear under My Certificates. Each entry has a View / Download button and a print option.

Training Discounts

Group discounts apply automatically — the more delegates you enrol, the greater the saving. Discounts are calculated at 3% per 5 delegates, scaling up to 40% off for 100+ delegates.

Delegates Discount
5 3% off
10 6% off
15 9% off
20 12% off
25 15% off
30 18% off
50 30% off
75 35% off
100 40% off

3% discount per 5 delegates, up to 40% off for 100+ delegates. Contact us for a custom group quote.

Upcoming Training Sessions
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Training Discounts
Delegates Discount
5 3% off
10 6% off
15 9% off
20 12% off
25 15% off
30 18% off
50 30% off
75 35% off
100 40% off

3% off per 5 delegates, up to 40% for 100+

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