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CLINICAL DATA MANAGEMENT & ANALYTICS |
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| Feasibility/Site Selection Process Ripe For Improvement | Article/Paper | By Life Science Connect Editorial Staff | One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how? |
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| 6 Ways Lab Data Can Improve Clinical Trials | Article | Quest Diagnostics | Explore six key ways laboratory data strengthens the clinical trial process, focusing on how RWD enhances patient recruitment, accelerates screening workflows, and improves overall study outcomes. |
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| Data Monitoring Committee (DMC) Services | Datasheet | Advarra | Let us build and manage your data monitoring committee or data safety monitoring board, ensuring oversight and the highest standards of data integrity and participant safety throughout your study. |
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| Regulated Document Review | Product | Ideagen | Enables secure real-time document review, co-authoring, and redaction in order to shorten the document review process by up to 65%. |
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CHOOSE YOUR OWN ADVENTURE |
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| You're receiving the Friday edition of the Clinical Leader newsletter, focusing on Clinical Data Management & Analytics and Trial Monitoring. 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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