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Webinar
Pioneering Progress for Rare Lives: Cell and Gene Therapy Trials in Pediatric Rare Disease Populations


White Paper
Precision medicines for neurodegenerative disorders: optimizing clinical development
15 February 2025
Case Study
Successfully delivering an ultra-rare disease clinical trial in a competitive landscape
15 February 2025
Case Study
Collaborative practices advance a rare ophthalmological disease clinical trial
15 February 2025
White Paper
Considerations for pediatric vaccine trials in developing countries
10 February 2025
White Paper
Qualified infectious disease product designation: What's to GAIN?
10 February 2025
Case Study
Navigating a dynamic study design in hepatitis B research
5 February 2025
Case Study
Successfully delivering an ultra-rare disease clinical trial in a competitive landscape
4 February 2025
White Paper
Recognizing the “new normal” of patient-centric clinical studies
4 February 2025
White Paper
A new era of the clinical trial: How immuno-oncology advances are reshaping traditional clinical development paradigms
4 February 2025
White Paper
Continuous innovation delivers faster, more efficient clinical trials
4 February 2025
Case Study
Innovative approaches help recruit and retain patients in a rare disease hematology study
4 February 2025
White Paper
Designing an optimal long-term follow- up program for gene therapies and genetically modified cell therapies
4 February 2025
White Paper
Optimizing clinical trials for pediatric obesity treatment
4 February 2025
White Paper
Incorporating the voice of patient in pediatric assent forms
4 February 2025
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