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| Webinar: Ensuring Effective Pharmacovigilance Regulatory Intelligence with FSP Partnerships | Pharmacovigilance (PV) is a critical component of drug and medical device development and commercialization, and effective PV regulatory intelligence (RI) ensures that PV is executed accurately and cost-effectively. Join us to examine several PV RI capabilities that differentiate top-tier FSP PV partners from other service providers and discover what it takes to stay on top of constantly changing regulatory requirements. Click here to learn more. |
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CLINICAL TRIAL TECHNOLOGY |
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| Vaccine Trial Sees >90% eCOA Adherence | Case Study | Medable | Here, we addressed vaccine trial challenges and drove remarkable success, achieving over 90% adherence to eCOA, ensuring active engagement from participants, and yielding consistent trial data. |
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| How eConsent Delivers Value For Sponsors | Article | By Vinita Navadgi, IQVIA Technologies | Review data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials. |
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CHOOSE YOUR OWN ADVENTURE |
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| You're receiving the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial Technology. 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)
Learn more about our personalized newsletters here. |
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