White paper

From Data to Emotion: The Power of Storytelling in Healthcare Communication

From Data to Emotion: The Power of Storytelling in Healthcare Communication

Healthcare Storytelling – Emotional Bridges between Science and Humanity

In an increasingly complex healthcare environment, traditional communication approaches are reaching their limits. Trust, empathy, and clarity have become key success factors—particularly in the pharmaceutical and healthcare industries. This is precisely where healthcare storytelling makes a difference.
 
The whitepaper provides a concise overview of how scientific information can be transformed into compelling and emotionally engaging communication. It conveys the core psychological and narrative principles behind effective storytelling and summarises how authentic stories can strengthen trust and credibility in the healthcare sector.
 
It serves as a compact guide for organisations that wish to establish storytelling as a strategic element—both internally and externally—to build meaningful bridges between science and humanity.

Download now the white paper 'From Data to Emotion: The Power of Storytelling in Healthcare Communication'.

We wish you many valuable insights as you read.


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White paper

From Data to Emotion: The Power of Storytelling in Healthcare Communication

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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

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Qualification Course: Head of Pharmacovigilance

- Combination of three compulsory seminars plus one elective module for (future) Heads of the Pharmacovigilance Department - Learn the responsibilities and legal aspects of managing a PV system and its staff, and select an elective module according to your individual interests.

online 01/01/2025 - 31/12/2026
Qualification Course: Qualified Person for Pharmacovigilance (QPPV)

- Combination of three selected seminars - With this qualification course, you will first gain insight into the legal aspects and general responsibilities of the Qualified Person for Pharmacovigilance (QPPV). You will then deepen your professional and practical knowledge to perform your role more effectively.

online 01/01/2025 - 31/12/2026
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 01/09/2025 - 31/12/2026
e-Learning: GDP - Basic Training

This e-Learning programme will provide you with knowledge on Good Distribution Practice in today's pharmaceutical industry

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online 31/12/2025
e-Learning: GDP - Basic Training

This e-Learning programme will provide you with knowledge on Good Distribution Practice in today's pharmaceutical industry

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online 31/12/2026
e-Learning: Medical Device Advisor §83 MPDG

Our e-learning, specially tailored for medical device advisors, provides you with the essential knowledge to navigate your professional duties confidently and in full legal compliance.

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e-Learning: Refresher Medical Device Advisor §83 MPDG

Our e-learning, specially tailored for medical device advisors, provides you with the essential knowledge to navigate your professional duties confidently and in full legal compliance.

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e-Learning: Medical Devices Basics - A Quick Introduction

Gain essential knowledge for your entry into the medical device industry in just 90 minutes! Understand regulations, market access, and vigilance with our compact e-learning.

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Abonnement: PharmaFORUM Webcast International

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.

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The EU Qualified Person for Pharmacovigilance (EU QPPV)

This two-day course equips new or in future QPPVs with the fundamentals of EU pharmacovigilance legislation, QPPV responsibilities, and strategic planning. Learn what it takes to fulfil the role, ensure compliance, and build your roadmap to QPPV readiness. Ideal for aspiring QPPVs or those preparing future candidates. Secure your place today!

online 13 - 14/01/2026