Registration Header
REGISTER TODAY!

Start Date: 10/6/2021
Start Time: 4:00 PM CEST
Duration: 35 minutes

The evaluation requirements for Nitrosamines in medicinal products have evolved over the last 3 years. For API, this is an essential topic.
Join us to hear about the changing Nitrosamine regulations, and learn our critical three-step approach: Risk Assessment, Confirmatory Testing & Change for Marketing Authorization.

During the webinar you’ll learn:
  • The history of Nitrosamine impurities
  • Principles behind the guidelines and Teva api's vision
  • How to avoid Nitrosamines in all medicinal products

Complete the form on the right-hand side of the page to register and save your seat.

If you're already registered for the Nitrosamines: A Moving Target , click below:

ALREADY REGISTERED?

Speakers

Diana Van Geenhoven

Head of Global Compliance at Teva api

Diana has a MSc degree in Chemical Engineering from University of Groningen (NL). She has worked in different function and companies and works for Teva api’s for 4 years and is currently Head of Global Compliance at Teva api.

Lena Lerman

Sr. Director Lifecycle Management at Teva api

Lena holds a Ph.D. degree in Organic Chemistry from Bar-Ilan University. She has worked in Teva api’s R&D for 14 years and is currently a Head of Lifecycle Management at Teva api.

Vesna Prgomet

Dir. Global Regulatory Affairs at Teva api

Vesna has 15 years of experience in pharma Regulatory Affairs and have been in Teva for 4 years. She has a bachelor's degree in chemistry and an MBA. She is currently Director Global Regulatory Affairs at Teva api.
First Name
Last Name
Email Address
Company
Job Title
Country