How to handle Reference Standards - Webinar Recording

How to handle Reference Standards - 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 Frank Böttcher, GMP-Consulting, Germany

Background

Reference standards are one of the key aspects in a Quality Control laboratory in the pharmaceutical industry. Correctly qualified reference materials are required to ensure valid QC results, which are the basis for a batch release by a QP.  Because of this, the handling and usage of the correct standard is important.

Target Group

This webinar is designed for all persons working in Quality Control departments or contract laboratories. It will be of interest in particular for personnel from Quality Assurance departments as well as Auditors and Qualified Persons of pharmaceutical companies, suppliers and consultants.

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

This webinar will give you a comprehensive overview of the GMP-compliant handling of reference standards. Regulatory requirements as well as the qualification and procurement of the reference standards will be discussed and explained.
  • Primary standards, Working standards, Ph. Eur. standards
  • Specific requirements and handling advices
  • How to handle Ph. Eur. standards in the daily business?
  • Qualification
  • Procurement
 
Recording from 02 July 2020
Duration of recording: about 1,5 h

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