GMP-Webinar: Expiry Dating for Chemicals, Reagents, Solutions, and Solvents: Requirements and Practical Implementation

Wednesday, 29 April 2015, 14.00 – 15.30 h CEST

Course No. 10333

header-image

Speakers

Dr Joachim Ermer
is Head of Quality Control Services Chemistry Frankfurt (Sanofi, Germany), and Global Reference Standards Coordinator of Sanofi. He studied biochemistry at University of Halle and has about 25 years’ experience in pharmaceutical analytics including development products, global responsibilities as Director of Analytical Processes and Technology, and Head of Quality Control. He is member of the USP Expert Panel on Validation and Verification and of the EFPIA Quality by Design working group.

Background

According to cGMP regulations, analytical procedures must be designed to assure that pharmaceuticals conform to appropriate standards of identity, strength, quality, and purity (21 CFR 211.160). This includes that components of these procedures such as reagents, solvents, mobile phases, and standard solutions are sufficiently controlled to maintain the required quality for an accurate testing. Therefore, appropriate instructions for preparation and storage must be established, as well as an expiry date (EU GMP Guide Part 1 Chapter 6: Quality Control and FDA Q&As on Current Good Manufacturing Practices).

Target Group

The webinar targets executives and staff in quality control laboratories and quality assurance, who want to get an overview on GMP requirements with respect to expiry dating of chemicals, reagents, solutions, and solvents, as well as their efficient practical implementation.

Programme

This webinar will provide recommendations how to establish expiry dates of reagents and solutions used in analytical procedures. Approaches range from literature-based information to specific stability studies, according to the risk of the respective component for the accuracy of the test procedure.

Practical aspects:
What are the documentation and labelling requirements?
Which approaches are suitable to establish an expiry date?
How can a risk-evaluation be performed to justify an appropriate expiry date establishment?
Practical examples for a scientifically sound stability evaluation of solutions used in quantification.






This training/webinar cannot be booked. Send us your inquiry by using the following contact form.

To find alternative dates for this training/webinar or similar events please see the complete list of all events.

For many training courses and webinars, there are also recordings you can order and watch any time. Just take a look at the complete list of all recordings.

* also payable by credit card
American Express Visa Mastercard

icon
Further dates on-site
Further dates on-site
Not available
icon
Further dates online
Further dates online
Not available
icon
Recording
Not available

Do you have any questions?

Please contact us:
Tel.: +49 6221 8444-0
E-Mail: info@gmp-compliance.org

Woman with headset

Go back

Testimonials about our courses and conferences

“Fantastic course – I really enjoyed the interactive structure & greatly appreciate social activity.”

Anthony Cummins, Sebela Pharmaceuticals, Ireland
GMP Auditor Practice, September 2023

 

“Very well organized, information on point without being overwhelming.”

Eleni Kallinikou, Pharmathen
Live Online Trainng - Pharmaceutical Contracts - Febuary 2024

 

“Good overview of different types of agreements, good to see both the GMP and the legal angle”

Ann Michiels, Johnson&Johnson
Live Online Trainng - Pharmaceutical Contracts, Febuary 2024

 

 

“Well prepared presentations and good presenters. I also like the way of asking questions.”

Alexandra Weidler, Hookipa Biotech GmbH, Austria
Live Online Training – QP Education Course Module A, November 2023