High Performance Liquid Chromatography (HPLC)

Analytical Method Development and Validation

Structured guidance for evaluating HPLC methods, instrument components, and laboratory evidence needed to support reportable analytical results under FDA and EPA expectations.

EXCLUSIVE: Get your team to

attend for just $ 390.

Individual registrations available too.

COURSE OVERVIEW & STRUCTURE

HPLC data depends on validated method performance.

Laboratories need clear judgment on when analytical results are supported by method evidence, instrument performance, and chromatographic system reliability. The session organizes key HPLC method characteristics, instrument validation elements, and audit-relevant evidence into a practical laboratory review structure.

The session moves from the relationship between analytical procedures and chromatographic systems into instrument components, method performance characteristics, and documentation expectations. It separates method validation from instrument validation while showing how both support data usability, audit readiness, and reliable laboratory reporting.

WHAT YOU’LL LEARN

Proving HPLC data is reportable

Instrument validation for pumps, columns, detectors, and data systems
Accuracy and precision assessment for HPLC methods
Repeatability, reproducibility, ruggedness, and robustness
Detection limits, quantitation limits, and linearity
Selectivity, specificity, and interference evaluation
Method and instrument evidence under FDA expectations

WHO SHOULD ATTEND

Designed for professionals involved in generating, validating, reviewing, auditing, or relying on regulated laboratory data.

Laboratory Operations

Analytical Chemistry

Quality Control

Quality Assurance

Validation

Regulatory Affairs

Quality Auditing

Compliance

FACULTY

Dr. John C. Fetzer

Dr. John C. Fetzer brings more than 35 years of liquid chromatographic method development experience, supported by doctoral research in chromatography and extensive publication in LC separations. His background in GLP accreditation, ISO 17025 compliance, and laboratory training makes him well suited to address both HPLC method performance and instrument validation expectations.

AFTER YOU REGISTER

Everything related to your course lives in one place.

FDB2324

After you register your seat, our team organizes everything for you; from access to certification – “from one place”.

You receive a confirmation and your course appears instantly in your TalkFDA dashboard.
Your course page becomes your central hub where you can join the session, access materials, and manage your learning.
At the scheduled time, simply click Join Session and you’ll be connected to the live Webex session with the instructor.
After the session, the playback becomes available on the same course page so you can revisit important sections.
Complete the course and your certificate is unlocked automatically in your learning history.

◙

For Teams Seeking Deeper Implementation Support

Customized training is also available through

TalkFDA Elite Training Labs.

This topic can also be delivered as a customized session through TalkFDA Elite Training Labs for organizations seeking structured, implementation-focused training aligned with their internal processes and quality systems.

Elite Training Labs sessions are tailored for teams and delivered in formats designed to support application, discussion, and practical integration beyond the live webinar format.

High Performance Liquid Chromatography (HPLC)

Analytical Method Development and Validation

🏠︎