Clinical Technologies Webinars

  1. Ready for eSource? Preparing For The Future Of Clinical Research

    Enhancing your data entry and monitoring and, as a result, strengthen your competitive edge. With eSource poised to become the next standard in clinical trial technology, the time is now to prepare for a new era in our industry.

  2. How to Leverage Clinical IRT To Improve Clinical Trial Efficiency Webinar

    This webinar will focus on the many attributes that must be considered to improve your clinical trial efficiency and experience. Participants will learn how to use the information you have from the protocol and clinical trial knowledge, along with clinical IRT expertise to ensure that the simple or complex randomization scheme is properly designed and set up to ensure flawless execution.

  3. How Linear Clinical Research Accelerated Trials Timelines And Improved Global Collaboration With eSource

    Explore the ways Medrio eSource has enabled Phase 1 clinical research unit improve global collaboration and accelerate trial timelines.

  4. Detecting, Handling, And Reporting Data Falsification, Misconduct, And/Or Suspected Fraud

    Whether indications of fraud appear as missing documentation, altered numbers, signatures that don’t match, or unavailable medical records Clinical research associates (CRAs) must be aware of the many signs of possible fraud or fabricated data occurring at a clinical trial site. This webinar explains the signs to look for and the proper protocol to handle and report the misconduct during each monitoring visit.

  5. eCOA, Patient Centricity And The Path To More Accurate Data

    Adopting a patient-centric focus in your trial is known to lead to more engaged patients and higher quality, more accurate clinical data. 

  6. Optimizing eConsent For Patient Centricity

    Use of electronic consent can help improve the current paper document approach, but there is more to it than just replacing paper with a multi-media eConsent. What does it take to make eConsent patient centric?

  7. What Happens After Your Device Is Approved? Collecting Data In The Real World

    In this presentation, Medpace Medical Device experts discuss key considerations for generating real-world evidence and how to apply critical insights in order to drive late-stage clinical research.

  8. Beware The Hidden Costs Of Conducting Clinical Trials: Understanding The Landmines And How To Avoid Them

    In this webinar, we explore four areas that can dramatically affect the cost and timelines of your clinical program and offer insight into elimination and control of these hidden landmines.

  9. Decisions For Your Next Trial: When To Adopt The CDISC Data Standard

    Trial sponsors must carefully plan their data consolidation and analysis strategies not only in preparation for CDISC-compliant submissions, but to respond to market influences and evolving clinical partnership models.

  10. How To Boost Disclosure Efficiencies With Outsourcing

    In this webinar, you’ll hear about exciting new advisory and managed disclosure services from TrialScope, including: compliance, policy and process assessments, as well as plain-language summaries, protocol registration, results posting, and redaction services.