Clinical Leader Webinar

31. Avoid Rescue Studies, Reduce Costs And Timelines & Accelerate Clinical Operations With Metrics 4/3/2020

    You can’t manage what you don’t measure. Having technology which can automate or assist in the timely monitoring of trials is a huge improvement over the status quo of manual methods such as spreadsheets, which are cumbersome and erroneous, not to mention only provide a dated snapshot of trial performance.

32. New Paradigm For Clinical Management Systems 3/31/2020

    The usual approach of adding technology and headcount to manage today’s clinical trials is not sustainable or scalable. In this webinar, Nick Dyer (CEO, Catalyst Clinical Research) discusses the challenges his team has experienced with complex early phase oncology studies, and why they chose Medidata’s CTMS to help Catalyst attain operational success.

33. Almac’s Webinar Series: Clinical Trial Supply And Technology 3/5/2020

    Download Almac’s on demand webinar series that discusses the multitude of efficiencies gained when harmonizing the clinical supply chain and tips for simplified supply planning. Follow the life cycle of the physical clinical supply chain from bulk manufacture to destruction, demonstrating the effective use of integrated digital systems for site, drug and patient management.

34. Ensuring Quality And Risk Mitigation With Proactive Planning In Clinical Trials 2/27/2020

    Emphasis on quality is everywhere, but in particular, the study startup portion of clinical trials is a hotspot, as it is pivotal to improving study conduct overall. With unrelenting pressures to rein in budgets and cycle times, stakeholders are turning to quality as a solution, starting with building it into study startup and bringing change to entrenched silos that stall trial operations. But how do Good Clinical Practice guidelines and systems improve overall study quality?

35. The Importance Of Contemporariness And An Approach To Mitigate Audit Findings 2/27/2020

    Contemporariness is not just isolated to the trial master file, it presents a problem to multi-country studies spanning numerous regulatory agencies. In an attempt to address the issue of contemporariness, sponsors and contract research organizations (CROs) have relied on resource-heavy and costly time-stamping of all incoming site correspondence to start the measure — but does this address regulatory concerns?

36. Will Decentralized Clinical Trials Compound Patient And Data Quality Risks? 2/27/2020

    With the introduction of a DCT, a significant element of patient engagement is moved away from a controlled (physical) investigator and site environment, which will present significant patient and data quality risks. This webcast will focus on understanding these risks and how they can be mitigated.

37. PLS Perspectives: Sponsor, Author & Regulatory Viewpoints 2/24/2020

    In this informative webinar, Jazz Pharmaceuticals will provide tips on launching a PLS program. A medical writer from ClaritiDox will give an overview of PLS best practices. And TrialScope’s chief strategy officer will share – and analyze – results from TrialScope’s recent PLS survey.

38. Building A Clinical Trials Website For Multiple Audiences 2/24/2020

    Thinking of (re)launching a clinical trials website? This webinar reveals why EMD Serono made this project a priority, how CISCRP helped guide patient-friendly content, and how TrialScope technology pulled it all together.

39. Insights in Pharmaceutical Manufacturing, Clinical Research and Technology 2/13/2020

    ISR conducted approximately two dozen pieces of research for syndication in 2019. This summary highlights learnings from these projects, and provides real, usable data for 2020 activities.

40. Three Keys To Successful Global Sample Processing 1/31/2020

    Sample preparation and processing are crucial steps in immuno-oncology, cell-based and gene therapies, and diagnostics. In this webinar, we discuss proper sample collection and transport, leveraging a global network of labs vetted for high-quality processing, and successful delivery to essential global storage for all sample types.