Participants will be asked to take part in a focus group about their perspectives on the usability of an informed consent toolkit to help improve the safe inclusion of pregnant and breastfeeding people in research.

Inclusion Criteria:

• 18-55 years of age
• Pregnant or breastfeeding while participated/ are participating in a clinical trial, considering participating in a clinical trial, or want/wanted to participate in a clinical trial.
• Able to participate in a focus group in English or French

Compensation will be provided for participants’ time.

To learn more or take part visit www.pregtrial.ca or contact pregtrial@rimuhc.ca