Are you ready to comply with the new European Pharmacopoeia (Ph. Eur.) revised text on extraneous agent testing in immunological veterinary medicinal products (IVMPs)?
The approach to extraneous agent testing in IVMPs has recently been updated and manufacturers of these products are required to comply with new standards from 1 July 2020. The EDQM is organising two free webinar sessions to help Ph. Eur. users ensure they are ready to use this new approach before the implementation date.
Register today to take part in our free webinar sessions!
The morning session will cover topics such as a summary of the revised Ph. Eur. requirements for extraneous agent testing, and what has changed and why, with a particular focus on risk management. This will be accompanied by concrete examples on how to apply the new approach.
The afternoon session will focus on the European regulatory landscape. Participants will have the opportunity to learn from representatives of regulatory authorities about the impact of the new approach on existing products and on best ways to apply the new approach, with the opportunity for IVMPs manufacturers to provide feedback and put forward questions.
These webinars will allow participants to get a better understanding of future expectations for extraneous agent testing. Participants can also send their questions in advance using the question form (deadline: 27 March 2020). Don’t miss out!
See also: