Resources

Patient engagement has evolved into a holistic approach that prioritises meaningful connections.

Pharma marketing to Black and African American communities: bridging health gaps with tailored outreach

Pharma marketing strategy: Crafting wellness connections in the digital age

Marketing strategies in the pharmaceutical industry: Crafting patient-centric campaigns

Black health disparities: Bridging the gap for brighter futures

3 tips to consider when highlighting patient diversity for your clinical trial awareness materials

Achieve Clinical Trial Diversity by Eliminating Bias and Introducing Cultural Safety

The Importance of a Thank You in Clinical Research

Harnessing the power of patient co‑creation

Why we need to enhance gender and sex diversity in clinical trials

Leave no-one behind: Why the language we use is crucial

The time is now: A closer look at the DEPICT and DIVERSE Trials Act

Steps towards breaking down religious and cultural barriers to clinical trial participation

How do we build trust in clinical research?

Demand Diversity: More than a movement.

My degree apprenticeship journey

Together we can…Clinical Trials Day 2023

The road to EDIRA is a road less travelled

Breaking down walls: Enhancing inclusive patient engagement

Is health technology as damaging for certain patient communities as it is beneficial to others?

Why creativity, innovation, and disruption can improve healthcare outcomes

Three barriers to participation of minoritized communities in clinical research, and how to overcome them

Strategic patient retention — how do we enable participants to stay on clinical research studies?

Navigating the uncharted: my rare disease reality

Introducing our new series: The A–Z of Health Research Equity

A–Z of Health Research Equity: A is for Accessibility

Ethics 101: The ethics of diversity in clinical trials

A–Z of Health Research Equity: B is for Biology

Beyond the veil: Unravelling implicit bias and the Muslim experience

Leveraging social media and influencers for ethical clinical trial recruitment

A-Z of Health Research Equity: C is for Co-Creation

Navigating the maze of health disparities and clinical trial participation in Europe

A–Z of Health Research Equity: D is for Diversity

A–Z of Health Research Equity: E is for Engagement

How cultural safety boosts clinical trial patient recruitment

A–Z of Health Research Equity: F is for Feedback

The UK’s push for evidence of patient engagement in ethics submissions for clinical trials

A–Z of Health Research Equity: G is for Goals

The impact of socioeconomic factors on clinical trial participation: A global and local perspective

A–Z OF HEALTH RESEARCH EQUITY: H IS FOR HISTORY

Leveraging digital platforms to engage underrepresented communities

How Can We Measure Diversity in Clinical Research?

FDA diversity action plan guidance: Is it a significant shift in clinical trials?

Patient advocacy groups and co-creation in clinical trials

A–Z of Health Research Equity: I is for Involvement

Ethical considerations in collecting ethnicity data for health research

A–Z of Health Research Equity: J is for Jargon

Why patient co-creation during the drug lifecycle is essential

Blog Post: K is for… Knowledge Transfer Partnership

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