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| Why The EU Biotech Act Matters To The U.S.: A Clinical Perspective | Guest Column | By Jessica Cordes, Clinical Excellence GmbH | The EU Biotech Act has across-the-pond implications, especially for U.S.-based biotech sponsors developing advanced therapy medicinal products (ATMPs, also called cell and gene therapies), oncology therapies, or other high-complexity modalities. Consultant Jessica Cordes explains. |
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| Study Analysis – Site Payment Automation | Case Study | Block Clinical Inc. | By removing administrative bottlenecks, see how automation improves cash flow for sites, reduces operational burden for sponsors, and supports smoother, more predictable trial execution. |
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| Optimizing Site Activation To Accelerate Clinical Trials | White Paper | By Rosie Whittaker, Reiz Evans, and Silvia Santos, PPD Clinical Research Business of Thermo Fisher Scientific | Clinical trial site activation delays are a major bottleneck in drug development, hampering trial timelines and funding flows. To reverse this trend, site-focused solutions are being prioritized. |
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| Working (Well) With Patient Advocates: The Sponsor POV | Guest Column | A conversation with Aeovian Pharmaceuticals, Allison Hulme, Ph.D. | Aeovian CEO Allison Hulme reflects on Aeovian Pharmaceuticals' partnership with the TSC Alliance and how it’s informed research and development of their first-in-class selective mTORC1 inhibitor. |
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| You're receiving the Monday edition of the Clinical Leader newsletter, focusing on Clinical Sites, Patient Centricity, and Patient Recruitment. To make changes to your newsletter selections, update your topic preferences. - Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
- Clinical Trial Technology (Tuesday)
- Decentralized Trials | Trial Management (Wednesday)
- Outsourcing Models | Regulatory & Compliance (Thursday)
- Clinical Data Management & Analytics | Trial Monitoring (Friday)
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