Back Module 3: Impurity control in the Ph. Eur.

EUROPEAN PHARMACOPOEIA 5 December 2024 - 10:00-11:30 (CET, France) live webinar
  • Diminuer la taille du texte
  • Augmenter la taille du texte
  • Imprimer la page
  • Imprimer en PDF
Module 3: Impurity control in the Ph. Eur.

Impurity control is an essential aspect of quality control in individual monographs of the Ph. Eur. In this module, you will learn about the Ph. Eur. policy for impurity control. It will cover all types of impurities, whether organic, inorganic (including elemental impurities), solvents or DNA-reactive impurities such as N-nitrosamines.

You will also learn about the analytical procedures used, the process of specification setting, the correct use of reference standards and how the different texts of the Ph. Eur. complement each other. In this context, the implementation of the relevant ICH guidelines and their importance for the Ph. Eur. will also be discussed.

The presentation will be followed by a live Q&A session.

Programme (subject to change):

10:00-11:00 Impurity control in the Ph. Eur.: theory and practical examples

11:00-11:30 Live Q&A Session

Register now

REGISTRATION FEES

All the training modules (webinars) are free of charge.

Places are limited, so sign up today!

Each registered participant will receive a copy of the presentation slides and the link to the webinar recording, which they can refer back to if needed in the future.

HOW TO REGISTER

The registration link is given under each module.

Participants can register to attend all the modules OR a selection of individual modules.

After registration, you will receive an invitation telling you how to access the webinar and how to test the system beforehand. On the day of the webinar, click on the link in the registration confirmation e-mail.

You can also check your system’s compatibility automatically.

Before registering, please read the Terms of Supply for EDQM Events.

Technical requirements
Help