Validation in Pharmaceutical Analysis: Calibration (Linearity) - Webinar Recording

Validation in Pharmaceutical Analysis: Calibration (Linearity) - Webinar Recording

Costs

ECA-Member*: EUR 199,--
Regular Fee*: EUR 249,--

(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

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 just 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

The webinar 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 succesful 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

Besides regulatory expectations, the Webinar series provides practical recommendations and orientation for demonstration of the suitability of analytical procedures. A rational and efficient validation approach is ultimatly 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.

The following topics will be covered in the part „Calibration“:
  • Regulatory requirements
  • Correlation or calibration?
  • Requirements to calibration models (linear single-point and multiple-point calibration, non-linear calibration, standard addition, internal calibration)
  • Suitable strategies to validate calibration models (linearity)
  • Statistical calculations (regression, suitable parameters)
  • Acceptance criteria for calibration function (residual and sensitivity plot) and ordinate intercept
 
Recording from 29 July 2020
Duration of recording: about 1,5 h.

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