Strategies for Effective Global Lifecycle Management Across Key Regulatory Regions
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Webcode 26012510
Dr. Christina Juli
Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany
Head of CMC Management CMB Dr. Christina Juli studied pharmacy at the University of Wuerzburg, Germany. After her PhD thesis in the fields of pharmaceutical chemistry, in 2012, she joined the ratiopharm GmbH in Ulm, Germany. She started her professional career as Senior Manager in the department of EU Regulatory Affairs Generic Maintenance. Since 2018, she is working in the Tech RA department at Boehringer Ingelheim Pharma GmbH & Co. KG in Biberach, Germany. In her role as Head of CMC Management CMB, she focuses on the CMC development for biologics and is responsible for the definition, compilation and review of the CMC documentation for clinical trial and new drug applications as well as for post approval submissions worldwide. Beyond that, as regulatory intelligence responsible for her business unit, she monitors the regulatory legislation, regulations, guidelines and position papers from pharmaceutical and biological industry worldwide. She is an active participant in the BioPhorum Operations Group (Post Approval Strategy and Regulatory Governance working groups).
Laia Canamero Ruiz
Asphalion, S.L., Barcelona, SPAIN
Regulatory Affairs Officer Laia Cañamero studied biotechnology at the Rovira i Virgili University of Tarragona, Spain. She joined Asphalion, S.L in 2019 Since then, she has been working in the lifecycle management of human medicinal products in Middle East and Central America, among other responsibilities. She has experience performing all the required regulatory activities with local partners, which gave her wide a vision of the regulatory framework in these regions.
Carmen Bas Jiménez
Senior Regulatory Affairs Officer at Asphalion, Barcelona
I am pharmacist working as a Senior Regulatory Affairs Officer at Asphalion, within the Life Cycle Management team. I have almost five years of experience in the Pharmaceutical Industry. My experience is based on the compilation, update, and review of dossiers at EU and International levels, specializing in other regions such as Latin America, Asia Pacific, and Middle East, as well as submission management in US and CA. Also, I previously worked as a Regulatory Affairs Associate at the company Chemo, which is one of the different business areas that belongs to the Insud Pharma Group.
21/01 - 11/02/2026
21/01 - 11/02/2026
21st January, 28th, 4th and 11th February 2026
live webcast from 10:00 am - 12:00 pm, Q&A session after each webcast
You may dial in 30 minutes before the training starts
online
online
Veranstaltung - 1,290 € zzgl. MwSt.
The participation fee includes downloadable documentation, a certificate of attendance, access to the Learning Space, comprehensive technical support, a pre-meeting session, and recordings of the webcasts.
Veranstaltung - 1,290 € zzgl. MwSt.
The participation fee includes downloadable documentation, a certificate of attendance, access to the Learning Space, comprehensive technical support, a pre-meeting session, and recordings of the webcasts.
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de
Global variations and lifecycle management - covering key regions: USA, Asia (China, Japan, South Korea), LATAM (Central America, Brazil), and Gulf Cooperation Council (GCC). Take this opportunity to discuss your specific daily business challenges with our experts and network with peers to see how others approach similar issues!
This webcast series, delivered in four sessions of two hours each, provides an in-depth understanding of the complexities in global lifecycle management.
Our highly experienced speakers will explain how to plan and implement variations on a global scale and collaborate effectively with local partners on ongoing lifecycle responsibilities. The focus is on key regions: the USA, Asia (China, Japan, South Korea), LATAM (Central America and Brazil), and the Gulf Cooperation Council (GCC).
Practical examples will cover both small and large molecule product classes.
By the end of this webcast series, you will be equipped to manage global lifecycle processes efficiently.
21.01.2026 10:00 - 12:00
28.01.2026 10:00 - 12:00
04.02.2026 10:00 - 12:00
11.02.2026 10:00 - 12:00
Please send us your questions concerning the seminar topics in advance.
We will be happy to forward them to the speakers, so that they know about your training requirements even better and are able to answer your questions at the seminar.
Please send your questions to v.planitz@forum-institut.de.
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You can attend one of our pre-meetings and explore our Learning Space free of charge. Registration is not required. You can find available dates for a pre-meeting in your customer portal. Click the green ‘Participate’ button in the pre-meeting in the customer portal and you will be redirected to the Learning Space.
The pre-meeting gives you the opportunity to explore our Learning Space and to familiarise yourself with the technology to start off your online training on the right foot. This is a non-binding offer for all our customers and not a prerequisite for participation. If a pre-meeting date does not suit you but you would still like a technology check, please contact us.
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