Sites STREAM

1. Should Sponsors Provide Source Document Templates? 12/9/2025

   Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.

2. Helping Sites Get Paid Frequently, Accurately, And With Full Visibility 8/5/2026

   By streamlining both automated and site-submitted invoicing workflows, this platform removes administrative friction, keeping the focus on trial progress and participant care.

3. What Does Site Engagement Actually Do? 4/29/2026

   Site Engagement stays close to research sites, providing guidance, reducing administrative strain, and addressing issues early. Their support keeps studies moving by preventing small operational challenges from becoming delays.

4. Accelerating Clinical Trials Through Streamlined Confidential Disclosure Agreements 2/9/2026

   In this presentation, Dr. Christine Senn addresses the persistent challenge of study startup delays by focusing on a primary legal hurdle: the Confidential Disclosure Agreement (CDA).

5. Using Technology To Reduce Monitoring Costs And Increase Quality 2/18/2025

   Join industry experts as they discuss how the true value of DDC lies not just in the cost of the technology itself but in the operational efficiencies it unlocks.

6. Agentic RTSM That Takes A Study From Kickoff To UAT 8/5/2026

   Discover how automated micropayments eliminate site paperwork, give participants instant access to funds, and provide real-time trial insights.

7. Automatically Triggered Micropayments And Built-In Reporting 8/5/2026

   Automated micropayments and unified trial data ease site burdens, boost participant retention, and deliver real-time insights. Discover a better way to run clinical trials.

8. Tailored Sponsor Engagement Key To Unlocking Site Network Efficiency 4/25/2025

   Karri Venn, VP site advocacy and mentorship at SCRS, emphasized the importance of sponsors recognizing the structure and capabilities of larger site networks.

9. Effective Study Design And Execution Of Renal And Hepatic Impairment Trials 5/1/2026

   Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired populations.

10. The Advantages Of Conducting Early Phase Trials In North America 10/24/2023

    In this webinar, Altasciences discuss the similarities and differences of conducting early phase research in North America versus other geographic regions.