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Welcome to the HL7's BRIDG wiki page.

The project scope statement was approved by RCRIM on August 18, 2009.

BRIDG Project Scope

BRIDG Project Scope revised 2010/01/28


Teleconference Minutes for 2011-07-25

Teleconference Minutes for 2011-04-25

Teleconference Minutes for 2010-06-28

Teleconference Minutes for 2010-03-29

Teleconference Minutes for 2010-02-22

Teleconference Minutes for 2009-11-30

Teleconference Minutes for 2009-10-26


The BRIDG Listserve is

To subscribe to this service, go to the HL7 Listservices Welcome Page

  1. Select Subscribe to List Services
  2. Fill in Name, Organization, e-mail and password
  3. Select type of mail
You receive copies of messages posted to the list as they are delivered and distributed (most common method)
Each night, around 12:00 am, you will receive a single email message containing all the messages contributed to the list that day. At the top of the message will be a numbered list of the subjects in that digest, followed by the complete messages themselves. Digest recipients will not receive messages sent to segments.
Digest with Attachments 
The same as a digest, but in MIME format so that the individual messages' formatting is preserved. Some email clients such as Outlook will show the digest as a series of attachments. Digest recipients will not receive messages sent to segments.
  1. Scroll down the list to Regulated Clinical Research Information Management
  2. Check bridg BRIDG Harmonization
  3. Scroll to the bottom of the page and check the confirmation statement
  4. Press Request Subscription

You will receive an e-mail confirmation. Follow the instructions on the email to activate your account. Once an account has been confirmed you can mail to the listserv using the mailing address

BRIDG Harmonization Process

BRIDG Harmonization Process and Procedure

Information on BRIDG

The BRIDG Model is a collaborative effort of stakeholders from the Clinical Data Interchange Standards Consortium (CDISC), the HL7 Regulated Clinical Research Information Management Technical Committee (RCRIM TC), the National Cancer Institute (NCI), and the US Food and Drug Administration (FDA) to produce a shared view of the dynamic and static semantics that collectively define a shared domain-of-interest, i.e. the domain of clincial and pre-clinical protocol-driven research and its associated regulatory artifacts.

Information on BRIDG can be found at