December 5-6, 2022
In-Person, Philadelphia, Pennsylvania
7th VirtualClinical Trials

With more clinical trials switching to fully decentralized and hybrid models, the need for a collaborative information exchange is more important than ever. At the 7th Virtual Clinical Trials Conference, hear actual case studies from current decentralized trials and discuss the future state of clinical research from top industry experts at the forefront of clinical trial designs. Explore what is working successfully and what obstacles you can avoid in data compliance, regulatory compliance and novel submission methods.
This is the industry’s leading, longest-lasting and most trusted conference on decentralized trials, offering you exclusive insights our speaking faculty hasn’t shared anywhere else! Join us in December for all-new insights on constructing and measuring endpoints, executing effective patient recruitment strategies, applying innovative technologies – and much more!
“The lessons presented actually reflected on examples of implementation and the lessons learned”
Innovation Manager – BAYER
“I wanted to understand more about where other pharma companies are in the process of building up these platforms, this exceeded my expectations”

As DGE welcomes you back to in-person conferences, we assure you that every precaution will be taken to keep you safe and healthy at our events. We have set new protocols for social distancing, onsite cleansing, and vaccination guarantees, all to make sure you have the best possible experience for learning and networking with a community of your peers.

  • VACCINATION IS MANDATORY to participate in a DGE in-person event. All event staff, speakers, attendees, sponsors, and exhibitors must submit proof of vaccinated status upon first entry to the event space
  • All event staff, speakers, attendees, sponsors, and exhibitors must wear masks in all event spaces, except when speaking on stage or eating in designated socially-distanced locations
  • All participants must affirm that they are not experiencing symptoms, have not been to an area with a travel health advisory, and have not been closely exposed to anyone who was
  • All events will follow federal and local safety guidances, as well as additional regulations that may be in place for each venue
  • All seating and exhibition areas will allow for 3 feet of space between participants
  • Event staff will be constantly monitoring room capacity and density
  • New directional and distancing signage will help remind participants about social distancing while keeping foot traffic flowing smoothly
  • All event spaces will have enhanced cleaning protocols throughout your stay
  • DGE and hotel staff have been trained on rapid response if event participants begin to show symptoms of illness

We appreciate your trust and your willingness to resume in-person learning. We pledge to put your health and safety first while holding our educational conferences, and to continue to refine and improve those standards based on developing guidelines from governments and venues.

Top Reasons to Attend

Topics covered will include:


  • Optimize Decentralized Trial Design and Operational Procedures
  • Establish Effective Vendor Management Procedures
  • Robust Endpoint Selection
  • Prioritize Nimble Approaches to Remote Monitoring Procedures
  • Maximize the Output of Hybrid Trial Execution
  • Review Advanced Solutions for eConsent
Top Reasons to Attend
  • Reduce the burden on patients, and therefore improve retention and reduce the trial’s overall cost
  • Alleviate site visits with proven hybrid approaches to accelerate timelines and allow for faster data gathering
  • Ensure regulatory and process improvements are implemented to reduce workload for clinical trial sites, resulting in time and cost efficiencies
  • Integrate effective technologies into trial design to omit the slowdown of the trial process
  • Enhance safety monitoring, safety producers and follow up outcomes
Who Should Attend
This event is designed for pharmaceutical, biotech, and medical device professionals responsible for:
  • Clinical Trials
  • Decentralized Trials
  • Trial Design
  • Remote Monitoring
  • Patient Recruitment
  • Patient Experience
  • Patient Solutions
  • Clinical Projects
  • Clinical Operations
  • Clinical Data
  • Clinical Supply Chain
  • Clinical Trial Supply Management / CTSM
  • Clinical Technology
  • Clinical Research
  • Clinical Sciences / Clinical Scientific Affairs
  • Digital Strategy
  • Chief Digital Officer
  • Chief Technology Officer
  • Data Manager
  • Site Solutions
  • R&D
  • Outsourcing
  • Operational Strategy
  • Clinical Regulatory Affairs
  • Clinical Safety
  • Medical Advisors
  • Medical Affairs
  • Clinical Processes
  • Clinical Systems
  • Scientific Affairs
  • Digital Health
  • Clinical Project Scientist
  • CQA Auditor
  • Clinical Development
  • Clinical Affairs
  • Business Development
  • Regulatory Affairs
  • Procurement Manager
  • Strategy and Innovation
  • Site Manager
  • Information Technology
  • Quality Planning
  • Digital Engagement
  • Medical Affairs
  • Medical Director
  • Technical Solutions
Event Sponsors
New Topics
Event Association Partners
Event Partners
Contact Us