White paper

AI in Pharma and Healthcare

AI in Pharma and Healthcare

Created with STORM by Stanford University, edited by Dr Henriette Wolf-Klein

AI in Pharma & Healthcare: Hype or Reality?

Artificial Intelligence was long hailed as the revolutionary force that would transform the pharmaceutical and healthcare industries. But now that the initial excitement has settled, what’s left of the big promises? Which AI applications have actually made a difference, where are the biggest hurdles, and what comes next?

Find the answers in our latest whitepaper: “Current Implementation of AI Applications in the Pharmaceutical and Healthcare Industry.”

This whitepaper, created with STORM by Stanford University and edited by Dr Henriette Wolf-Klein, offers a clear and concise overview of real-world AI applications – from accelerating drug discovery and optimizing clinical trials to improving diagnostics and enabling personalized medicine.

Discover which technologies have proven themselves in practice, where the industry still faces challenges, and how ethical and regulatory questions are shaping AI adoption today. Real-life case studies and emerging trends help you separate lasting innovation from fleeting hype.

Download your copy now: “Current Implementation of AI Applications in the Pharmaceutical and Healthcare Industry.”

We hope you find the content insightful and engaging.





 

Download

White paper

AI in Pharma and Healthcare

Download

Download

Once you have completed the following fields, you can download the desired content. Alternatively, log in to your customer portal. The document will then be freely available to you.
I agree that the FORUM Institut may contact me to inform me about events and relevant content.
I can revoke my permission at any time.
3 + 1 =   

Events “

Do filter
Sort
Tiles
Lists
Qualification course: CMC-Specialist in Regulatory Affairs

With this qualification course, you can continue your education in a structured manner in all CMC topics, with a technical focus on development methods, manufacturing processes, CMC documents, change management, and much more.

online 01/01/-31/12/2025
Your pre-meeting: Be prepared for your event

Attend one of our free pre-meetings to familiarise yourself with the Learning Space and the various ways in which you can interact during the event

online
Webcast series: Global regulatory requirements for drug device combination products (DDCs)

Global regulatory requirements for drug device combination products (DDCs): You will receive a regulatory overview for the EU, the US, China, MENA, Mexico and other LATAM countries, plus you will obtain tips and tricks by (local) experts on how to speed up the approval process.

online 29/04/-27/08/2025
International Medical Device Regulations

This online course offers an in-depth overview of the medical device approval process in key global markets: Regulatory strategies, approval steps and timelines for global market access, with a focus on North and South America, the Asia-Pacific region and China.

online 26-27/06/2025
Pharmaceutical Law in Germany and Related Regulations

Join our one-day seminar on pharmaceutical law to gain a comprehensive overview of the key legal and regulatory principles in Germany and the EU. No prior legal knowledge is required.

online 30/06/2025
European Patent Drafting Camp: Chemistry, Pharma, and Biotech

Our speakers will give you tips and tricks on EP claim drafting and will show you which pitfalls to avoid.

online 01-02/07/2025
Recent Decisions of the EPO Boards of Appeal in Biotechnology and Biopharmaceuticals

The most important decisions of the Boards of Appeal in the field of biopharmaceuticals and biotechnology and changes in the Guidelines will be presented. The panelists will discuss, in particular, the consequences of these decisions and changes on patent practice.

online 03/07/2025
The GVP Refresher

The Good Pharmacovigilance Practices modules (GVP modules) by the European Medicines Agency (EMA) serve as a reference for standard practices in pharmacovigilance. This online course serves as a refresher and ensures that you are up to date with the best practices.

online 03-04/07/2025
Artificial Intelligence in Pharmacovigilance

Join our interactive course to explore how AI is transforming pharmacovigilance. Take part in discussions, hands-on workshops, and case studies while diving into AI technologies, regulations, and their applications in drug safety. Register now to participate, share insights, and collaborate with peers!

online 10/07/2025
online 19/01/2026
GCP for ATMP

Are you involved in the planning and conduction of clinical trials with ATMP? Do you require current knowledge on the latest GCP guideline (ICH E6 (R3)) AND ATMP-specific considerations? Then join this seminar to stay informed (including training certificate)!

online 05/08/2025
Regulatory Affairs and GMP compliance in Eastern Europe

This online training offers comprehensive insights into Regulatory Affairs, CMC, and GMP requirements, with a focus on the latest updates and developments in EAEU countries.

online 28-29/08/2025