Abonnement: PharmaFORUM Webcast International
"Electronic Product Information (ePI): Global Developments and Regulatory Perspectives" 12 November 2026
- Experts with local know-how
- High-level knowledge transfer
- We are following the IMI quality criteria
Abonnement
Ab
1.100,00 €
zzgl. MwSt.
Leistungen & Ablauf
Veranstaltung - 1.100,-€ zzgl. MwSt.
Membership is valid for one year. The annual membership fee of €1,100 (plus German VAT) is payable upon registration. Membership is automatically renewed for a further year unless written notice is submitted no later than six weeks before the end of the current membership period. A 12-month membership may begin at any time.
We also offer group accounts. For €1,990 (plus German VAT), you and your colleagues can watch together in a conference room via a single shared account (certificates not available). For €2,500
(plus German VAT), you receive up to five individual accounts, each with the option to receive a certificate. For €3,750 (plus German VAT), you receive up to ten individual accounts, each with the option to receive a certificate.
Buchungsdetails
Abonnement
Ab
1.100,00 €
zzgl. MwSt.
Leistungen & Ablauf
Veranstaltung - 1.100,-€ zzgl. MwSt.
Membership is valid for one year. The annual membership fee of €1,100 (plus German VAT) is payable upon registration. Membership is automatically renewed for a further year unless written notice is submitted no later than six weeks before the end of the current membership period. A 12-month membership may begin at any time.
We also offer group accounts. For €1,990 (plus German VAT), you and your colleagues can watch together in a conference room via a single shared account (certificates not available). For €2,500
(plus German VAT), you receive up to five individual accounts, each with the option to receive a certificate. For €3,750 (plus German VAT), you receive up to ten individual accounts, each with the option to receive a certificate.
Stay informed with updates from our global and local experts, who will provide the latest regulatory and legislative insights every two months. In 2026, topics will include CMC documentation, regulatory intelligence, regulatory pathways in Africa, enrichment of PMS product data, global regulatory reliance models and ePI.
Your speaker
Dr. Niklas Jänich
Boehringer Ingelheim International GmbH, Ingelheim, GERMANY
Head of Global Labeling Operations & Digitization;
Dr. Jänich is an expert in Regulatory Affairs with extensive expertise in the field of…
Your speaker
Dr. Niklas Jänich
Boehringer Ingelheim International GmbH, Ingelheim, GERMANY
Head of Global Labeling Operations & Digitization;
Dr. Jänich is an expert in Regulatory Affairs with extensive expertise in the field of labeling. In his role, he is responsible for the labeling process as well as associated systems, compliance, and digitalization. Furthermore, he advances the development and implementation of Structured Content Authoring and electronic product information in the GxP-regulated environment.
What to Expect
- The evolving complexity of CMC documentation in global submissions
- Regulatory Intelligence in a Global Context
- Regulatory Pathways in Africa - Updates and Challenges
- Obligations 2026 towards the EMA for the enrichment of PMS product data
- Global Reliance Pathways: ACCESS, ORBIS and OPEN in Focus
- Electronic Product Information (ePI): Global Developments and Regulatory Perspectives
Who Should Attend
This webcast series addresses the needs of managers in the pharmaceutical industry, who need to keep up to date in global regulatory affairs.
Objective of the Event
Do you work in international regulatory affairs? We would like to invite you to join our live webcasts, where local regulatory affairs experts will inform you every two months of the latest news and trends in global marketing authorisation.
You will meet our experts in a virtual conference room and share your experiences in regulatory affairs within and beyond the ICH region.
Each meeting will be held as a 1.5-2-hour webcast, presenting the latest news with supporting presentation slides. To be best prepared, you will be able to download the complete presentation documents prior to each webcast.
Are you unable to attend one of the webcasts? No problem! Following each live meeting, you will be able to retrieve the recorded webcast (audio track and presentation) from our eLearning Centre, using your personal password. This allows you to review each presentation at any time and as often as you like.
Your Benefit
- Live broadcasts every two months on current worldwide regulatory affairs topics
- Continuing education at your workplace
- Lectures also available online at any time
- Direct communication with the experts
Downloads
Request the documents using our form.
Brochure
Weitere Informationen
More details
Find all the details regarding the programme, experts and technical requirements at
www.forum-institut.com/pharma-webcast-international.
Your benefits
- Six live webcasts with international experts per year
- Recorded presentations at our e-Learning Centre to review as often as you like
- Documentations for your personal download
- Multiple Choice Test after each webcast to obtain a personal certificate
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Further Information
Technical requirements
Here you can find the technical requirements for our online events that must be met.
e-Learning - Click and learn
We provide flexible education and training with high-quality e-Learning programmes for several topics.
Quality guaranteed!
our feedback produced as result of 1.7 in 2022. Thank you!
Your Contact Person
We are happy to advise you personally and individually.
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de