Featured Webinars

31. Creating A New World In Clinical Trial Feasibility Utilizing Advanced Analytics 11/26/2024

    Citeline utilizes several data resources to enhance feasibility strategies and help clients drive patient engagement and recruitment.

32. Citeline SmartSolutions 11/11/2024

    Citeline SmartSolutions is a new generation of AI-powered clinical solutions including tools to recommend primary endpoints and inclusion/exclusion criteria and instantly generate a list of protocol-matched investigators for your trial.

33. Investigator SmartSelect 10/23/2024

    This advanced recommendation engine identifies protocol-specific investigators in just minutes, dramatically shortening a process that typically takes four to six weeks.

34. What Is Citeline Connect? 9/24/2024

    Explore a centralized patient recruitment platform that enables sponsors to meet their enrollment goals using a diverse selection of channels and recruitment partners.

35. Optimize Protocols For More Successful Trials 9/17/2024

    Find out how you can harness the power of AI and world-class data to recommend endpoints and inclusion/exclusion criteria for streamlined protocol design that results in more positive trial outcomes.

36. Citeline Patient Engagement & Recruitment Solutions 8/20/2024

    Our patient-centric solutions and services enable the collection, analysis, and application of data to drive informed decisions across clinical, commercial, and regulatory domains.

37. Streamline The Clinical Trial Disclosure Process 7/29/2024

    Core Data simplifies the registry submission and approval process by consolidating data for multiple registries into one single form, promoting consistency across registries and saving time by minimizing data entry.

38. TrialScope Intelligence 7/16/2024

    This easy-to-use platform reduces the risk of clinical trial disclosure noncompliance by tracking global disclosure regulations for you. Browse comprehensive regulatory authority and trial registry requirements.

39. Plain Language Summaries Becoming A Mandate Worldwide 6/13/2024

    A growing number of countries are requiring clinical trial protocol and results disclosures to be written in plain language, influencing how these documents are authored.

40. Navigating The Clinical Trial Diversity Maze 5/15/2024

    Gain comprehensive insights into diversity action plans in clinical trials through this informative presentation, focusing on the latest FDA guidelines for collecting race and ethnicity data.