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


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Considerations for pediatric vaccine trials in developing countries
10 February 2025
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Qualified infectious disease product designation: What's to GAIN?
10 February 2025
ケーススタディ
Successfully delivering an ultra-rare disease clinical trial in a competitive landscape
4 February 2025
ホワイトペーパー
Recognizing the “new normal” of patient-centric clinical studies
4 February 2025
ホワイトペーパー
A new era of the clinical trial: How immuno-oncology advances are reshaping traditional clinical development paradigms
4 February 2025
ホワイトペーパー
Continuous innovation delivers faster, more efficient clinical trials
4 February 2025
ケーススタディ
Innovative approaches help recruit and retain patients in a rare disease hematology study
4 February 2025
ホワイトペーパー
Designing an optimal long-term follow- up program for gene therapies and genetically modified cell therapies
4 February 2025
ホワイトペーパー
Optimizing clinical trials for pediatric obesity treatment
4 February 2025
ホワイトペーパー
Incorporating the voice of patient in pediatric assent forms
4 February 2025
ブログ
Future-Proofing SaMD: Regulatory Strategies for Medical Software Development
4 February 2025
ブログ
Detecting the Undetectable: The Rising Potential of Liquid Biopsies in Oncology
31 January 2025
ブログ
Key challenges in pediatric vaccine trials in low- and middle- income countries
29 January 2025
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