Recording Online Training: Lifecycle Concept and Precision

Recording Online Training: Lifecycle Concept and Precision

Costs

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

(All prices excl. VAT)

* also payable by credit card American Express Visa Mastercard

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. A rational and efficient validation approach is ultimately based on the respective routine application, which should be reflected in the validation design. This includes the identification of the relevant performance parameters, the selection of appropriate tests and calculations and, in particular, the establishment of acceptance criteria for the evaluation.

Background

According to EU GMP Guide Part 1, Chapter 6, Quality Control (6.15) and US 21 CFR 211.194, analytical procedures must be suitable for their intended purpose. The regulatory requirements to validation of analytical procedures utilised for release and stability studies of drug substances and drug products are described in the ICH guideline Q2(R1). However, its degree of detail is rather low, and the discussion is mainly focused on chromatographic methods. The latter is one of the reasons for the started revision of the guideline, as well as inclusion of lifecycle and risk management aspects, which gained increasing attention in the last years.

Target Group

This Training is aimed at executives and employees from Quality Control, Quality Assurance, and regulatory who want to gain a better understanding of the GMP requirements as well as current trends and are interested in practical recommendations for an efficient design, execution, and evaluation of a successful analytical validation.
 

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.

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 for Analytical Procedures
  •  ICH Q2-Guideline – requirements and gaps
  •  ICH Q2-Revision and Q14 Development of Analytical Procedures (intended changes and content)
  •  USP Draft: The Analytical Procedure Lifecycle
  •  Requirements to the analytical performance (Analytical Target Profile)
  •  Verification of compendial procedures
Performance Attributes of Analytical Procedures
  •  Validation characteristics and error types
  •  Distribution of analytical data
  •  Evaluation of performance parameters (simple, statistical)
  •  Efficient validation
Precision
  •  Precision levels (system precision, repeatability, intermediate precision, reproducibility)
  •  Acceptance limits for assay
    •  Derivation from probability, measurement uncertainty, tolerance factors
  •  Concentration dependency of precision (Horwitz function)
    •  Acceptance limits for impurities
  •  Design of precision studies and calculations
    •  Uncertainty of precisions: point estimators and confidence intervals
  •  Optimisation of precision by averaging (replication strategy)
    •  Precision of the reportable value (small molecules, bioassay)
    •  Assay for small molecules, bioassay
Workshop: Multiple Choice Questions (from Publications)
  •  How to avoid mistakes in validation

 

Duration of Recording: 2h 21min

Recording from 29 June 2021

 

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