May 18-19, 2022
In-Person, Philadelphia, Pennsylvania - Also being live streamed
6th 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 6th 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 May 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”

Vaccination is mandatory to participate in a DGE in-person event. All event delegates, speakers, sponsors, and staff must be prepared to show proof of vaccinated status upon first entering the event space. Mask-wearing is up to each individual’s discretion. Thank you for your help in making sure this remains a safe and healthy educational networking event!

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
  • Data Management
  • 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 Management
  • CQA Auditor
  • Clinical Development
  • Clinical Affairs
  • Business Development
  • Regulatory Affairs
  • Procurement
  • Strategy and Innovation
  • Site Management
  • Information Technology
  • Quality Planning
  • Digital Engagement
  • Medical Affairs
  • Medical Director
  • Technical Solutions
Event Sponsors
New Topics
Event Pricing
Event Association Partners
Event Partners
Contact Us