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The Fit-for-Purpose Gap: What RWD Still Gets Wrong

In this session, industry experts Dr. Radek Wasiak and Isabella Even-Chen break down the critical "Fit-for-Purpose Gap"—the misstep of assuming a single, generalized dataset can satisfy every study design, regulatory requirement, or health economics endpoint.

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Medical & Commercial

The Fit-for-Purpose Gap: What RWD Still Gets Wrong

World Orphan Drug Congress Europe: October 26-28 at the RAI Convention Centre in Amsterdam

Getting COA strategy right from the start: Early endpoint decisions that strengthen evidence and reduce risk

Education Spotlight: European Market Access University Diploma (EMAUD)

Prof. Dr. Wagschal - What can we expect from the upcoming elections in Germany?

Scientist.com Acquires InsideScientific

Supplier Spotlight: PicnicHealth

The Benefits of Multilingualism in the Workplace

Dr. Mathias Flume - AMNOG will change in 2022, but how?

Is Cost-Effectiveness Analysis Racist?

Life Science Startup Nightmares

Generating Evidence for Optimal Market Access: An Executive Interview with Jeff Anderson and Rosemary Jose, OPEN Health

Using Wearables Data to Support Drug Reimbursement: Challenges, Opportunities and Case Studies

Education Spotlight - Xavier Health Economics & Clinical Outcomes Research

Online Marketplaces and Multiple Value Propositions

Supplier Spotlight: Self Care Catalysts

Supplier Spotlight: Self Care Catalysts

Overcoming Clinical Research Challenges: Analyzing EHR Data to Replicate Clinical Trials and Construct External Control Arms

Getting the most from clinical experts in the time of COVID-19: Lessons learned

All About the "Value, Access and Evidence" Category

Catching Up With the NA3RsC

Revealing the Unknown: How the COVID Active Research Experience (CARE) Registry is Enhancing Community Health

Faster Science: HEOR, RWE & Market Access Sourcing

8 Ways to Optimize Your Lab Space

COVID-19 and Racial/Ethnic Disparities in Health

Obesity Webinar Series 2020

2020 Review of the Best Project Managers for EU-funded Projects

7 Everyday Activities to Engage Children With Science

Getting COA strategy right from the start: Early endpoint decisions that strengthen evidence and reduce risk

The Fit-for-Purpose Gap: What RWD Still Gets Wrong

Filling the Gap: Integrating Patient-Generated Data into Real-World Evidence

Closing Gaps in Care: Health Equity and the Inflation Reduction Act - A Cutting Edge Conversation

Network meta-analysis and its role in evidence-based decision-making

Sustainable Science: Transforming Pharma-Supplier Partnerships

Addressing Orphan and Rare Diseases - A Cutting Edge Conversation

Joint Clinical Assessment 2025: Pioneering Pathways for Oncology, Advanced Therapies & Rare Diseases

RWE reality check: Routine patient health records and regulatory requirements

"S" Stands for Systematic: Demystifying the Systematic Literature Review

Survival Analysis for Immature Data: A Review of Techniques and Lessons Learned

Market Access - Transforming BioTech Commercial Decisions?

The Scientific and Operational Elegance of Study Replication with Real-World EHR Data: A Vitiligo and Alopecia Example

Practical AI: Adding Insight to the Patient Journey with Digital Phenotyping

Insights from the 2024 Salary Survey Report by HealthEconomics.com

Beyond Accelerated Approvals: External Control Arms

Delphi Panels: What Are They Good For?

Unraveling European Animal Welfare Legislation for Biotech & Pharma

Patient Voices Matter: Transforming Industry-Sponsored Real-World Evidence with Patient-Centric Approaches

Integrated Evidence Generation Planning: Driving Successful Reimbursement and Life Cycle Management

Understanding Animal Welfare Best Practices in Asia Pacific for Biotech & Pharma

Strategies to Optimize Commercialization of Oncology Treatments for Younger Adults

Navigating Animal Welfare Legislation in North America: Insights for Biotech & Pharma

Navigating the Clinical Outcomes Maze: An Overview of Clinical Outcomes Assessments and Why Training Matters

EU HTA Joint Clinical Assessments: Navigating Potential Challenges Ahead of 2025

Cell & Gene Therapies - Beginning with the End in Mind

Bridging the Gap: Strategies for Patient-Centered Real-World Evidence in Rare Diseases

Integrating Patient Engagement and Trainee Development in Pre-Clinical Research

Pharma can target ultra-rare conditions ‚Äî the next step is financing them

Transforming Healthcare Using Big Data and Remote Monitoring

Partnering with Disease Registries: The Value and Impact for Real-World Evidence Generation

Minimizing the Impact of Cross-Cultural Differences in COA Translations

Synthesise RWE and AI. Transform patient-driven healthcare

Endpoints at #DIA23

Tracking and Measuring Market Access Performance

Certified Corporate Wellness Specialist(CCWS): Is It For Me?

L7|LIVE SF - Tuesday, June 13th, 2023

Transforming clinical research: Scaling real-world data across diseases with expert-led AI

Connected communities: Advancing population health through data and emerging technology

Improving Patient Outcomes: AI-Based Phenotyping for Diagnosis, Treatment, and Clinical Trials

The reimagined hospital: How health systems are keeping up with new tech

Clinical Trial Innovation: How Healthcare Technology is Evolving

How to assess the quality of AI output when structuring unstructured medical data

Driving value from healthcare data: How integrated cloud-based data is foundational to drive enterprise change

Advancing identity data management for digital engagement: How leading organizations are doing it

How Digital Health Can Empower Cancer Patients

Keeping up with demands for healthcare outside of the hospital: Critical ways tech supports the distributed care model

Closing the gaps of getting data to make decisions

Patient Data: Opportunities for Rare Diseases, Cell and Gene Therapies, and Oncology

Medicare Part D: Price Negotiation Panel Discussion

Notice of Pre-Application Webinar for RFA-AG-24-009, "Alzheimer's Disease (AD) and AD-Related Dementias (ADRD) Real-World Data Platform (U54 Clinical Trial Optional)"