Home / Resources / RWD: More Than Just Another Acronym
RWD: More Than Just Another Acronym

Citeline is the industry leader in clinical trial intelligence using RWD from multiple sources to help sponsors optimize trial design, more efficiently select trial sites and investigators, and accelerate patient enrollment.

Download the article.

PDF preview of the RWD More than Just an Acronym article by Citeline.
Citeline may contact you about relevant products, services and content. To opt-out of these communications or to manage what you receive, please visit our Preference Center.

Your information will be used in accordance with our Privacy notice.

Thank you.




Your download should open in a new window. You can also manually download by clicking the button below.
Relevant products
Citeline subscriber exploring the diversity feasibility using Global Patient Insights.
Global Patient Insights
Enabling sponsors to optimize investigator selection and hit diversity goals faster
Aerial shot of a diverse population, key to the success of the Diversity Action Plan.
Sitetrove Diversity Module
Enabling sponsors to optimize investigator selection and hit diversity goals faster
''
Investigator SmartSelect
Quickly generate a list of investigators best fit for your trial

Related resources

Aerial shot of a group of people.
Use Case
Clinical

Real World Data Resource Bundle

View three compelling use cases and discover how incorporating RWD into clinical trial planning and execution can foster patient centricity.

Thumbnail of the Supporting Diversity in Clinical Trial Recruitment Infographic PDF.
Infographic
Patient Engagement & Recruitment

Supporting Diversity in Clinical Trial Recruitment

See how the Citeline Connect Recruitment Collective partnership network drives study awareness and participation globally.

Transforming Patient Engagement-resource-card-thumbnail
SEP 01, 2023
Webinar
Patient Engagement & Recruitment

On-demand Webinar: Transforming Patient Engagement

Webinar - Transforming Patient Engagement: What It Takes to Operationalize a Seamless, Trustworthy Clinical Trial Experience

View all resources