Continuous Verification in Pharmaceutical Analysis - Online Training Recording

Costs

*ECA-Member:**	EUR 590,--
*Regular Fee:**	EUR 690,--
*EU/GMP Inspectorates:**	EUR 590,--
*APIC Member Discount:**	EUR 640,--

(All prices excl. VAT). Important notes on sales tax.

Registration

* also payable by credit card

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Speakers

Dr Joachim Ermer, Ermer Quality Consulting, Germany

Objectives

Besides regulatory expectations, this Live Online Training provides practical recommendations and orientation for demonstration of the on-going suitability of analytical procedures. In particular, efficient approaches will be presented to extract information and data from routine analysis. This will be illustrated with examples from quality control of chemical drug substances and biopharmaceuticals.

A comprehensive understanding of the real analytical performance is extremely helpful to investigate and evaluate suspect or out-of specification (OOS) results as well as for a continuous process Validation.

Background

According to the FDA-Guidance „Analytical Procedures and Methods Validation for Drugs and Biologics“, it should be continually assured that an analytical procedure remains fit for its intended purpose throughout its application. This includes an ongoing program for routine monitoring of analytical performance data, and the systematic evaluation of changes with the objective to evaluate regularly the need for optimization and revalidation, if needed. These activities belong to stage 3 of the analytical lifecycle management as discussed in the draft of the new USP information chapter <1220>. The on-going performance verification is also intended to be included in the revision of the ICH validation guideline Q2.

Target Group

This Live Online Training is aimed at executives and employees from Quality Control, Quality Assurance, and production who want to gain a better understanding of the GMP requirements as well as current discussions with respect to the lifecycle management of analytical procedures and are interested in practical recommendations for an efficient design, execution, and evaluation of a continuous analytical performance verification.

Technical Details:

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.

Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.

In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Please be aware: The recording does not include the Q & A sessions.

Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.

Programme

Regulatory Requirements and the Lifecycle Concept of Analytical Procedures

FDA validation guidance (monitoring and trending)
USP General information chapter <1220> (valid May 1st, 2022)
- Stage 1: Procedure Design and Development
- Stage 2: Procedure Performance Qualification
- Stage 3: Ongoing Procedure Performance Verificatio
ICH Q2-Revision and Q14 Analytical development

Workshop
Sources of data and information on analytical Performance

Evaluation of Procedure Performance

Indicators of performance (conformity, validity, analytical control parameters)
Risk-based identification of suitable performance parameters (SST, from sample analysis, control samples)
Evaluation of information and data (OOS, invalid results, control charts, average parameters)
Continual improvements

Monitoring and Trend Analysis

Control charts (Shewart, range, standard deviation, combined, CUSUM)
Pragmatic establishment of rules and limits (statistical, empirical)
Trend analysis for stability results
Examples

Recording from 03 May 2022

Duration of Recording: 2h 10min

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