Clinical Technologies Solutions

31. Oracle Health Sciences Data Management Workbench 5/20/2020

    Increasing data diversity and volume, as well as the manual processes required to collect, clean, and analyze data, delay trial timelines and increase costs. Additionally, there is overwhelming pressure for sponsors to get answers to their scientific questions faster. What if you had real-time access to your data, with the ability to identify issues and respond quickly?

32. eConsent Saves Time And Increases Patient Engagement In Clinical Trial Startup 9/2/2020

    Clinical Ink’s eConsent module is an all-in-one solution that optimizes your consent process for simpler study startup. Not only does it reduce site workload, saving you time and money, but it delivers a better patient experience.

33. Advarra eRegulatory Management System Overview 1/27/2021

    Streamline your regulatory process and think beyond the binder. Save time, improve workflows, and enhance regulatory compliance across your organization with a system designed for academic institutions managing a large volume of protocols.

34. Veeva Vault Clinical Data Management Suite 2/12/2021

    Do you need to accelerate study cycle times, run the study you want, and get get clean data faster? Veeva Vault Clinical Data Management Suite offers EDC, data cleaning, coding, and review in a single unified suite.

35. Laboratory Data Integration 6/9/2020

    Are you struggling with the integration and management of laboratory data? LabConnect understands the challenges of integrating laboratory data sets from various sources and in diverse formats. LabConnect is here to provide you with a solution: a unified dataset that can be customized to meet the needs of your systems and tools.

36. Clinical One™ Randomization And Supplies Management Cloud Service 5/20/2020

    Randomization and trial supplies management is critical to any clinical study. But traditionally, the technology used to support this process has put a painful lag on overall efficiency. What if you could take back control and shave weeks off the process?

37. Data Management And Cloud Solutions For Life Sciences 12/10/2020

    Compliance, Collaboration, Control: Streamlining the Development Process.

38. Veeva Vault eTMF Brochure 7/12/2019

    Veeva Vault eTMF provides real-time inspection readiness, full visibility into TMF status, and access for all study partners. Sponsors get the clarity they need to oversee trials more effectively. CROs gain the flexibility and control required to operationalize their SOPs and efficiently populate the eTMF. Auditors get easy online access with a dedicated role. And sites receive a simple and efficient means to interact with CROs and sponsors.Veeva Vault eTMF promotes the highest levels of  TMF quality, access, visibility, and control.

39. The 411 On Efficient Monitoring In Vault CTMS 11/19/2019

    Because monitoring accounts for 25-30% of overall trial costs,¹ life sciences companies and contract research organizations (CROs) are always looking for ways to optimize their monitoring processes. In this post, we’ll cover how the use of monitoring reviewer comments enables more efficient monitoring in Vault CTMS.

40. Meeting Post-Marketing Surveillance Requirements For New Vaccines In The COVID Era 1/5/2021

    With several promising COVID-19 vaccine candidates approaching regulatory approval, manufacturers are preparing for essential post-marketing evaluations of long-term safety and effectiveness in real-world patient populations. The unprecedented scale and criticality of current vaccine development demands modern, evidence-driven safety surveillance and monitoring solutions that capitalize on the benefits of today’s digitization of healthcare data. Powered by real world evidence (RWE), UBC’s surveillance solutions are uniquely equipped to ensure your organization’s readiness to meet the urgent post-marketing requirements of your new vaccine.