Educational Webinars

Upcoming Webinars:

In this webinar you will:

  • Understand why many congress investments fail to deliver lasting impact

  • Recognise the engagement gap between pharma teams and HCP expectations

  • Get introduced to a structured approach to pre-, during-, and post-congress engagement

  • Gain practical insights you can immediately reflect on within your own organisation

  • Benchmark your current congress approach against live industry feedback

 

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In this webinar you will learn:

  • The impact of AI and digital saturation on information processing and behavioural patterns

  • What current research reveals about cognitive overload, retention, and engagement

  • How digital-native patients evaluate credibility and trust

  • Why authenticity and storytelling are gaining strategic importance

 

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In this webinar you will learn:

  • What MFN pricing could mean in practice for global pricing and launch planning

  • Where the real risks lie for global teams across US and European markets

  • How different MFN policy scenarios could play out across markets

  • Practical approaches to stress-test your plans and anticipate downstream impact

  • How to build a more resilient, future-ready global launch strategy

 

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In this webinar you will learn:

  • Why analogue-based decision making is often deeply flawed

  • The vastness of “analogue space”

  • The impossibility of seeing what you actually need to see (such as net prices)

  • The psychology behind why teams are drawn to bad analogues

  • What works much better
     

For details & registration

In this webinar you will learn:

  • Why some launches stall despite strong clinical data

  • The difference between activity metrics and performance-driving KPIs

  • Simple principles for building a launch KPI dashboard
     

For details & registration

Recorded Webinars:

In this webinar you will learn:

  • Why AI cannot escape the need for value-for-money evidence

  • How AI’s impact can be evaluated through the “quintuple aim” framework (patient outcomes, patient experience, clinician well-being, cost, and equity)

  • How to assess value for money — and how these methods apply to AI

  • What recent systematic reviews reveal about the cost-effectiveness of AI in healthcare

  • Common shortcomings in current economic evaluations of AI solutions

  • Why a full Health Technology Assessment of AI in healthcare is needed

 

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In this webinar you will learn:

  • How AI is being applied — unevenly but increasingly — across BD workflows

  • Practical AI use cases for in-licensing: search, monitoring, due diligence

  • How AI can support out-licensing: partner identification, conference prep, negotiation readiness

  • Examples of tools and approaches BD teams are trying today

  • Key risks, limitations and common pitfalls

 

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In this webinar you will learn:

  • The shifts in HCP behaviour that explain declining attention and content fatigue

  • How to adopt a trust-based, inbound content model tailored for HCP needs

  • What “discoverability” means today, including the role of search and AI tools

  • Real-world examples of educational content that supports HCPs at the moment of need

 

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In this webinar you will learn:

  • A clear, non-technical explanation of agents, how they differ from “just ChatGPT”, and where they fit in your current commercial tools and processes.

  • A focused tour of high-impact use cases already feasible in pharma today: brand planning, content support and document retrieval, field coaching, and insight generation.

  • How to choose a strong first use case, map the workflow, define the system prompt and the knowledge base, turning a business problem into a working agent without overcomplicating things.

  • Open Q&A

 

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In this webinar you will learn:

  • The evolving AI landscape in pharma and medical affairs

  • Inside the AI toolbox: what’s possible (and what’s not)

  • Real-world case studies of AI solutions in pharma

 

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In this webinar you will learn:

  • How a “perfect” payer/prescriber interview should unfold, and why most interviews never achieve this.

  • The evidence, through actual AI vs human case studies, that shows how AI-moderated interviews can significantly outperform human moderators.

  • Outperformance means more insights and deeper insights that are measurable.

  • The psychology of why human respondents give more depth and more honesty when talking to an AI moderator.

  • What this means for the future of your pharma payer and prescriber research.

 

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In this webinar you will learn:

  • What is the biggest challenge faced by Medical Affairs?

  • What is driving the evolution of Medical Affairs and how does it affect us?

  • What are the key ambitions for Medical Affairs and what is its role in modern pharma?

  • How can this roadmap help to develop a positive culture of Medical Affairs Excellence?

 

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In this webinar you will learn:

  • Where and how AI can be integrated in the market access process

  • How AI-based tools can reduce time and resource demands in dossier writing

  • What HTA bodies and payers really accept when it comes to AI-supported evidence

  • Live demonstration of use cases in pricing, objection handling, and launch planning

 

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In this webinar you will learn:

  • What we mean by Medical Affairs impact: Defining and understanding the concept

  • The 5 pillars of Medical Affairs impact: A framework for driving success

  • Different perspectives on impact: Short-term vs. long-term, micro vs. macro, internal vs. external

  • Making your impact visible: Best practices for communicating value to internal stakeholders

 

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In this webinar you will learn how to optimally:

  • Allocate resources in a country across brands in an agile way

  • Allocate resources across tactics at brand level, ex ante and ex post

 

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In this webinar you will learn:

  • Simple alternatives to traditional conjoint methods that handle complex product profiles much more effectively

  • Alternative approaches that require smaller sample sizes

  • Leveraging the vast repository of over $50 million worth of published pharma conjoint studies

  • Why (unfortunately) you cannot survey ChatGPT instead of doing conjoints (Harvard academics have tried!)

 

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In this webinar you will learn:

  • What is better and what is more accepted: comparative RWE versus indirect comparisons based on trials.

  • Synthetic control groups and post-approval comparative RWE studies: How do they work?

  • Existing guidance and guidelines for comparative RWE studies 

 

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In this webinar you will learn:

  • How to personalise portfolio strategy at a country level as a component of near-term portfolio planning

  • How to align investment priorities when considering mid-term portfolio strategy  

  • How to manage uncertainty in the context of portfolio planning for the long term

 

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In this webinar you will learn:

  • Overview of the pharmaceutical value chain, a simple but powerful framework

  • How BD&L activities help leverage strengths and address weaknesses across the full value chain

  • Application of the value chain framework to assess strengths and weaknesses at each stage of the BD&L process

 

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In this webinar you will learn:

  • Using AI and/or econometrics to analyse past payer behaviour. Because, for payers, sometimes “actions speak louder than words”.

  • Using meta-analysis to uncover powerful predictions from the mountain of published research papers.

  • Using simulators of “virtual negotiations” to understand innovative contracting schemes from your and payers’ perspectives.

 

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In this webinar you will learn:

  • How to talk about value for money to clinicians and patient advocacy groups

  • How to align the clinical and the health economic view

  • How to go beyond the QALY to account for what matters to patients

  • How to deal with evidence gaps: the increasing role of Real World Evidence 

 

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In this webinar you will learn:

  • The key ways that cell and gene therapy do and do not differ from more “conventional” therapies.

  • The commercial significance of the fact that cell and gene therapies invariably enter the market with “one foot still in the lab” (i.e. with immature clinical data).

  • The vital importance of “hope-based therapy” (high levels of uncertainty) rather than “evidence-based therapy” and how customers (payers/prescribers) actually act when faced with these uncertainties. 

  • ...

 

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In this webinar you will learn:

  • The state of the art for measuring QALYs

  • The value of a QALY

  • Measuring health gains: beyond the QALY

 

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