Strategies for Effective Global Lifecycle Management Across Key Regulatory Regions
- Webcast guaranteed to take place! -
Webcode 26082511
Dr. Christina Juli
Boehringer Ingelheim International GmbH Biberach an der Riss, GERMANY
Head of CMC, CCM RA Office NBE 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 ratiopharm GmbH in Ulm, Germany and started her professional career as Senior Manager in the department of EU Regulatory Affairs Generic Maintenance. From 2018 to 2025, she was working at the manufacturing site for biopharmaceuticals in Biberach, Germany as Head of CMC Management CMB where she focused on the CMC development for biologics for the contract manufacturing business of Boehringer Ingelheim. In her current role as Head of CMC RA Office NBE, she focuses on the CMC development for biologics and is responsible for CMC regulatory topics of development projects, products, and strategic regulatory projects. Beyond that she is an active participant of several industry groups such as the BioPhorum Operations Group (Post Approval Strategy and Regulatory Governance working groups) or EFPIA.
Carmen Bas Jiménez
Asphalion, S.L., Barcelona, SPAIN
Senior Regulatory Affairs Officer Carmen Bas Jiménez is a pharmacist working as a Senior Regulatory Affairs Officer at Asphalion, within the Life Cycle Management team. She has almost five years of experience in the Pharmaceutical Industry. Her 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. She 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.
Maria Roncero Lendinez
Asphalion, S.L., Barcelona, SPAIN
Regulatory Affairs Consultant
María Roncero Lendínez studied Pharmacy from the Universidad Complutense de Madrid and has over nine years of experience in the pharmaceutical sector. She joined Asphalion S.L. in 2022. She has focused on the life-cycle management of medicinal products, ensuring regulatory compliance and coordinating submission processes across Europe, the Asia-Pacific region, and the Middle East. Her close collaboration with local stakeholders has enabled her to develop a comprehensive perspective of regulatory requirements in these areas.
More information please click here.
31/08 - 21/09/2026
31/08 - 21/09/2026
Live Webcasts
:
31 August 2026: 10:00 - 12:00
07 September 2026: 09:00 - 11:00
14 September 2026: 10:00 - 12:00
21 September 2026: 10:00 - 12:00
Q&A session follows each live webcast. Recordings will be available afterwards.
You may dial in 20 minutes before the training begins.
online
online
Event - 1,290€ plus tax
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.
Event - 1,290€ plus tax
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.
31.08.2026 10:00 - 12:00
07.09.2026 10:00 - 12:00
14.09.2026 10:00 - 12:00
21.09.2026 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.
FORUM Institut’s all-in-one training platform uses the latest teaching methods.
All our online training courses take place in the Learning Space, our holistic learning environment with many features that promote effective and sustainable learning.
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.
of 5 stars of all ratings from 2025
of 5 stars on Trustpilot = good
You as "beginner" or "refresher" would like to feel more secure writing CMC documents? Our experts will provide you with...
Sind Sie als RA-Professinal im Bereich der Marktzulassung für die Erstellung der Qualitätsdokumentation von pharmazeutis...
In diesem Seminar erhalten Sie Know-how zur Zulassung von Arzneimitteln in Europa. Sie lernen, welche Zulassungswege mög...
Profitieren Sie als Mitarbeitende*r im Bereich Qualität/GMP vom Praxis-Know-how unserer Experten und holen Sie sich Hilf...
Dieses Seminar richtet sich speziell an Fachkräfte aus der Pharmabranche, die im Bereich Qualitätsmanagement oder Regula...
