Demo Data

Study Setup Progress 2/3

Protocol

Upload and confirm protocol details

Configuration

Configure EDC forms and settings

Review and Export

Review and export to EDC systems

Email Alerts

An email alert within the Email Alerts configuration for the study.

Alert ID	Trigger Condition	Trigger Code	Condition Code Type	Email Subject	Email Body	Recipient	Source	Enabled Status	Error Message	Suggested Fix	Error Related CRF	Actions
					Dear {study name} Safety Team, {site_name} has reported an adverse event for {participant_id} that is serious and assessed as related to the study treatment. Please review the case details in the EDC and follow the SAE reporting SOP. Regards;		Uploaded
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Uploaded
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Manual
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Manual
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Leova from protocol
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Uploaded
					Dear {study name} Safety Team, {site_name} has reported an adverse event for {participant_id} that is serious and assessed as related to the study treatment. Please review the case details in the EDC and follow the SAE reporting SOP. Regards;		Uploaded
					Dear {study name} Safety Team, {site_name} has reported an adverse event for {participant_id} that is serious and assessed as related to the study treatment. Please review the case details in the EDC and follow the SAE reporting SOP. Regards;		Leova from protocol
					Dear {study name} Safety Team, {site_name} has reported an adverse event for {participant_id} that is serious and assessed as related to the study treatment. Please review the case details in the EDC and follow the SAE reporting SOP. Regards;		Leova from protocol
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Uploaded
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Manual
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Manual
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Leova from protocol
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Uploaded
					Hello {study name} Team, A low enrollment rate has been detected for the study. Site: {site_name} Please consider mitigation actions (site engagement, outreach, or protocol review). Regards,		Manual
					Hello {study name} QA/Clinical Team, A protocol deviation has been reported for participant {participant_id} at {site_name}. Please review details in the EDC and document required CAPA per SOP. Regards,		Manual

16 Email Alerts