Evaluating an eClinical Provider to Meet the Needs of Modern Trials

Life Sciences, Clinical Trials,
  • Monday, March 30, 2020

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
    • Patient-centricity
  • 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

Muhammad Bilal, Senior Director, Data Sciences, Medrio

Muhammad Bilal is the Senior Director, Data Sciences at Medrio with 16+ years of data management experience. During this time he has worked as a lead Data Manager and a lead EDC Programmer using a variety of EDC systems. His SDTM programing experience provides him with a good understanding of clinical database structure and requirements.

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:

  • CROs
  • Pharma
  • Biotech
  • Medical Device
  • Clinical Research Sites

What You Will Learn

Attendees will learn about: 

  • The current eClinical landscape 
  • How to classify vendors 
  • Clinical research trends, their technology and data needs

Xtalks Partner


Medrio is a leading provider of eClinical technology, including EDC, eCOA/ePRO, eConsent, and DDC for sponsors and CROs, supporting pharma, medical device, and diagnostics clinical trials since 2005.

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