Ethylene Glycol and Diethylene Glycol - Webinar Recording

Ethylene Glycol and Diethylene Glycol - Webinar Recording

Costs

ECA-Member*: EUR 249,--
Regular Fee*: EUR 299,--

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

* 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

Alexander Doppelreiter, CEO, Head QC of Reference Analytics

Background

In recent months, the awareness for the impurities ethylene glycol and diethylene glycol in pharmaceutical products was increased due to several warning letters issued by the FDA and a call for action by the WHO.

Ethylen glycol (EG) and diethylene glycol (DEG) are potentially harmful impurities that can be found in pharmaceutical products. The compounds are commonly used in industrial applications, such as in the production of plastics and solvents. However, their presence in pharmaceuticals is a cause for concern due to its toxic properties.

The presence of EG and DEG in pharmaceutical products can result from various sources, including improper sourcing of raw materials or cross-contamination in manufacturing equipment. Regulatory agencies around the world have set strict limits on the permissible levels of those impurities in pharmaceutical products to ensure patient safety.

Manufacturers are required to implement robust quality control practices, including thorough testing of raw materials and finished products, to detect and prevent contamination. Regular monitoring and adherence to regulatory guidelines are crucial to ensure that pharmaceutical products are free from harmful levels of these impurities, safeguarding the health of patients, who rely on these medications.

Target Group

This webinar addresses itself to all, which are involved in quality control of incoming goods, starting material or release of final drug product.
  • Analytical laboratory managers and their colleagues
  • Analytical scientists
  • QA, manufacturing and supply chain professionals

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 presentation will be made available as PDF-files via download during the online training course. After the successful completion of the online training, you are able to download the certificate of attendance.

Programme

This webinar will give a short overview of the impurities, possible sources and analytical strategies.
  • Content of current FDA warning letters
  • Guidance for Industry: Testing of Glycerin for Diethylene
  • Glycol and Ethylene Glycol
  • Possible sources of contamination
 
Recording from 16 November 2023
Duration of Recording: 1h 27min

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