Using Electronic Data Capture EDC and other eClinical tools such as electronic patient-reported outcome (ePRO), eConsent, and Direct Data Capture (DDC) has become the norm for the collection of clinical and patient-reported data in clinical research, however, there are 100s of varied eClinical platforms available to sponsors and Contract Research Organizations (CROs) and it can be difficult to ensure that you select the best fit for your study design during your evaluation process. Furthermore, as regulatory guidelines push for new methods of data collection and new clinical trial models emerge (hybrid/virtual trials), how do you select an eClinical provider capable of supporting you through the clinical trials of tomorrow?
Looking to the future, it is clear that Sponsors and CROs need eClinical platforms that allow for flexible clinical and patient-reported data collection, real-time data access and insights and give them the peace of mind they need to make strides in a changing environment.
During this free live webinar we will discuss:
- The current eClinical landscape, and how to classify vendors during your evaluation
- Clinical research trends and their associated technology and data collection needs
- Hybrid/Decentralized Trials
- Regulatory Guidelines
- How a Unified eClinical Platform offers benefits over a Traditional eClinical Platform, and how to select an eClinical provider that offers modern technology with a proven platform you can trust
Kathryn LaTendresse, Senior Director, Clinical Data Management, Synteract
Kathryn LaTendresse has over 18 years of data management experience in clinical trials, with experience across multiple therapeutic areas and all phases of development. She leads teams responsible for design and implementation of clinical technology and integrations. Given that the right technology solution is a key element of success, Ms. LaTendresse has years of experience in asking the right questions and making technology recommendations. Ms. LaTendresse participates in strategic governance and leadership teams to build and develop key client partnerships.Message Presenter
Gabriel Westerlund, Sales Engineer, Medrio
As a Solutions Engineer at Medrio, Gabe is the go-to technical expert for product demonstrations, customer implementations, trainings, and more. He holds a Bachelor of Science from Uppsala University in Uppsala, Sweden, and is based out of Medrio’s San Francisco headquarters.Message Presenter
Who Should Attend?
This webinar will appeal to individuals in the following roles:
- Data Managers
- Clinical Trial Site Managers
- Clinical Research Associates
- Clinical Operations
at the following organization types:
- Medical Device
- Clinical Research Sites
What You Will Learn
Attendees will learn about:
- The current eClinical landscape
- How to classifying vendors
- Clinical research trends and their technology and data needs
Medrio is the leading provider of eClinical technology for early-phase pharma, device, and diagnostics clinical trials. Founded in 2005, the company’s cloud-based EDC, eSource, eConsent, and ePRO solutions deliver fast, flexible, and easy-to-use tools for the collection and management of clinical data and patient-reported outcome responses. Study sponsors and contract research organizations have used Medrio extensively in clinical trials across a wide array of therapeutic areas, with notable success in oncology, infectious disease, and more. Medrio has extensive experience in all study phases and leads the market in early-phase trials. The company serves over 500 customers globally, with headquarters in San Francisco and offices in numerous domestic and international locations. For more information, please visit www.medrio.com.