Registration Deadline: Friday, August 15
Taking place in the US and Europe, this two-day interactive event will bring sponsor companies, clinical solution providers, and key industry stakeholders together to exchange knowledge in implementing digital protocols, standards, and solutions.
Attendees will:
- Connect and collaborate to build expertise in advancing DDF and the protocol digitalization journey—from planning and proof of concept to production readiness
- Learn how TransCelerate is catalyzing cross-industry collaborations to accelerate digital protocol adoption and ecosystem readiness through diverse use cases
- Gain insights into the change management journey and learn how to make the case for change to showcase DDF as a value driver within organizations
- Hear from sponsors, technical solution providers, and transformation leaders about key considerations in the protocol digitalization journey from planning to implementation
Choose from two locations:
- Novartis in New Jersey, US (1 Health Plaza, East Hanover, NJ 07936) We have reached capacity for this location. If you are interested in attending, please register and you will be placed on a waitlist.
- F. Hoffman-La Roche in Basel, CH (Grenzacherstrasse 124, 4070) We have reached capacity for this location. If you are interested in attending, please register and you will be placed on a waitlist.
Ideal attendees:
- Anyone interested in protocol digitalization and interoperability
- Sponsors and CROs
- Protocol development and authoring community
- Clinical trial study start-up and system set-up specialists
- Clinical trial digital and technology support
- Data managers, innovation managers, infrastructure managers, and programmers in clinical development
- Clinical data standard leads (e.g., data standards managers and data governance managers)
- Clinical trial technologists (e.g., solution architects, business analysts, and technology managers)
- Technology solution providers involved in clinical trials, such as:
- Study builders and authoring platforms
- Electronic data capture systems
- Clinical trial management systems and clinical data management systems
- Metadata repositories
- Interactive response technologies
- Central laboratories
- Health authorities
- Industry consortia/groups