Automate clinical research operations
Automate clinical research operations
Automate clinical research operations
Automate clinical research operations
Generate CRFs, AE reports, and disease registries from your longitudinal health records and study protocols.
Generate CRFs, AE reports, and disease registries from your longitudinal health records and study protocols.
Generate CRFs, AE reports, and disease registries from your longitudinal health records and study protocols.
Built for investigators, study coordinators, and clinical research teams.
Built for investigators, study coordinators, and clinical research teams.
Built for investigators, study coordinators, and clinical research teams.
FOSTER / RESEARCH WORKSPACE
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Patient records
Visit notes
Lab reports
Prior visits
AE report
Adverse event
Fatigue
Severity
Grade 2 · CTCAE v5
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Source-linked. Ready for review.
FOSTER / AE REPORT
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Patient records
Visit notes
Lab reports
Prior visits
AE report
Adverse event
Fatigue
Severity
Grade 2 · CTCAE v5
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Source-linked. Ready for review.
FOSTER / RESEARCH WORKSPACE
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Patient records
Visit notes
Lab reports
Prior visits
AE report
Adverse event
Fatigue
Severity
Grade 2 · CTCAE v5
SOURCE · VISIT NOTE
ECOG PS 2 · Generalized weakness
Source-linked. Ready for review.
Built for investigators, study coordinators, and clinical research teams.
Built for investigators, study coordinators, and clinical research teams.
How it works
How it works
How it works
How it works
Configure the forms and rules once. Apply them consistently as new records and patient visits arrive.
Configure the forms and rules once. Apply them consistently as new records and patient visits arrive.
FOSTER / STUDY WORKFLOW
FOSTER / STUDY WORKFLOW
01
Configure study
CRF template
Study arm
Required
Visit day
Required
Conditional logic
Define your study form fields and abstraction instructions.
Define your study form fields and abstraction instructions.
01
Configure study
CRF template
Study arm
Required
Visit day
Required
Conditional logic
Define your study form fields and abstraction instructions.
02
Add records
Source records
Visit note.pdf
Lab report.pdf
Prior visit.pdf
Input your longitudinal health records in your preferred format: API, scanned/handwritten notes, PDFs, text or clinical conversations.
Input your longitudinal health records in your preferred format: API, scanned/handwritten notes, PDFs, text or clinical conversations.
02
Add records
Source records
Visit note.pdf
Lab report.pdf
Prior visit.pdf
Input your longitudinal health records in your preferred format: API, scanned/handwritten notes, PDFs, text or clinical conversations.
03
Generate
Draft CRF
Study arm
Arm A
Visit day
Day 8
Symptom
Fatigue
Auto-populate your study outputs from the relevant patient records.
Auto-populate your study outputs from the relevant patient records.
03
Generate
Draft CRF
Study arm
Arm A
Visit day
Day 8
Symptom
Fatigue
Auto-populate your study outputs from the relevant patient records.
04
Review
Evidence review
Symptom
Fatigue
SOURCE · VISIT NOTE
“Patient reports fatigue.”
Validate with your team
Inspect supporting evidence, resolve flagged outputs, and validate the results.
Inspect supporting evidence, resolve flagged outputs, and validate the results.
04
Review
Evidence review
Symptom
Fatigue
SOURCE · VISIT NOTE
“Patient reports fatigue.”
Validate with your team
Inspect supporting evidence, resolve flagged outputs, and validate the results.
WHERE FOSTER FITS
WHERE FOSTER FITS
WHERE FOSTER FITS
WHERE FOSTER FITS
Built around your study’s forms, protocols, and review process.
Built around your study’s forms, protocols, and review process.
Cycle 2 · Day 8
Study arm
Arm A
Visit day
Day 8
Source record
Visit note
PROTOCOL-SPECIFIC
Every field, with its source
Case report forms
Populate protocol-specific forms from source records.
Cycle 2 · Day 8
Study arm
Arm A
Visit day
Day 8
Source record
Visit note
PROTOCOL-SPECIFIC
Every field, with its source
Case report forms
Populate protocol-specific forms from source records.
Cycle 2 · Day 8
Study arm
Arm A
Visit day
Day 8
Source record
Visit note
PROTOCOL-SPECIFIC
Every field, with its source
Case report forms
Populate protocol-specific forms from source records.
PATIENT EX 001
Track each adverse event across visits.
Adverse event
Visit 1
12 May
Visit 2
16 May
Visit 3
20 May
Fatigue
Grade 2
Grade 1
Resolved
Nausea
Grade 1
Resolved
Resolved
Rash
None
Grade 1
Grade 1
PATIENT EX 001
Track each adverse event across visits.
Adverse event
Visit 1
12 May
Visit 2
16 May
Visit 3
20 May
Fatigue
Grade 2
Grade 1
Resolved
Nausea
Grade 1
Resolved
Resolved
Rash
None
Grade 1
Grade 1
PATIENT EX 001
Track each adverse event across visits.
Adverse event
Visit 1
12 May
Visit 2
16 May
Visit 3
20 May
Fatigue
Grade 2
Grade 1
Resolved
Nausea
Grade 1
Resolved
Resolved
Rash
None
Grade 1
Grade 1
Update your registry as new records arrive.
New clinical record
Follow-up note · EX 004
↓
Cohort registry
Record
Diagnosis
Treatment
Follow-up
EX 001
Linked
Linked
Updated
EX 002
Linked
Linked
Updated
EX 003
Linked
Linked
Review
EX 004
NEW
Linked
Linked
Updated
Registries & cohorts
Build longitudinal datasets from historical and ongoing records.
Update your registry as new records arrive.
New clinical record
Follow-up note · EX 004
↓
Cohort registry
Record
Diagnosis
Treatment
Follow-up
EX 001
Linked
Linked
Updated
EX 002
Linked
Linked
Updated
EX 003
Linked
Linked
Review
EX 004
NEW
Linked
Linked
Updated
Registries & cohorts
Build longitudinal datasets from historical and ongoing records.
Update your registry as new records arrive.
New clinical record
Follow-up note · EX 004
↓
Cohort registry
Record
Diagnosis
Treatment
Follow-up
EX 001
Linked
Linked
Updated
EX 002
Linked
Linked
Updated
EX 003
Linked
Linked
Review
EX 004
NEW
Linked
Linked
Updated
Registries & cohorts
Build longitudinal datasets from historical and ongoing records.
STUDY RULE
Visit window
Day 8 ± 2 days
Visit recorded
Day 12
!
Potential deviation
Visit outside the configured window.
Flagged for study-team review
STUDY RULE
Visit window
Day 8 ± 2 days
Visit recorded
Day 12
!
Potential deviation
Visit outside the configured window.
Flagged for study-team review
STUDY RULE
Visit window
Day 8 ± 2 days
Visit recorded
Day 12
!
Potential deviation
Visit outside the configured window.
Flagged for study-team review
Demonstrated in real studies
Demonstrated in real studies
Demonstrated in real studies
Demonstrated in real studies
Foster supports commercial and academic research across clinical trial data management, cohort studies, and disease registries.
Foster supports commercial and academic research across clinical trial data management, cohort studies, and disease registries.
Tata Memorial Hospital
Trial data capture
Clinical
records
→
CRF
AE
CRFs +
AE reports
Tata Memorial Hospital
Trial data capture
Clinical
records
→
CRF
AE
CRFs +
AE reports
AIIMS Delhi
IBD cohort
Historical
records
→
IBD
IBD study
proformas
AIIMS Delhi
IBD cohort
Historical
records
→
IBD
IBD study
proformas
National Cancer Grid
Hematology registries
Longitudinal
records
→
Hematology
registries
National Cancer Grid
Hematology registries
Longitudinal
records
→
Hematology
registries
Measured impact
Study-specific results for correctness and documentation time.
AE REPORTING CORRECTNESS
94.3%
Medical professional
76.2%
Foster
94.3%
+18.1 percentage points
Source: AE reporting study · Status: under review
LOWER DOCUMENTATION TIME
79%
Manual workflow
6 min
Foster
1.28 min
Source: Ambient documentation study · ESMO AI & Digital Oncology 2025
OBSERVED HALLUCINATIONS
0
300 evaluated encounters
Source: Ambient documentation study · Tata Memorial Hospital
Measured impact
Study-specific results for correctness and documentation time.
AE REPORTING CORRECTNESS
94.3%
Medical professional
76.2%
Foster
94.3%
+18.1 percentage points
Source: AE reporting study · Status: under review
LOWER DOCUMENTATION TIME
79%
Manual workflow
6 min
Foster
1.28 min
Source: Ambient documentation study · ESMO AI & Digital Oncology 2025
OBSERVED HALLUCINATIONS
0
300 evaluated encounters
Source: Ambient documentation study · Tata Memorial Hospital
Measured impact
Study-specific results for correctness and documentation time.
AE REPORTING CORRECTNESS
94.3%
Medical professional
76.2%
Foster
94.3%
+18.1 percentage points
Source: AE reporting study · Status: under review
LOWER DOCUMENTATION TIME
79%
Manual workflow
6 min
Foster
1.28 min
Source: Ambient documentation study · ESMO AI & Digital Oncology 2025
OBSERVED HALLUCINATIONS
0
300 evaluated encounters
Source: Ambient documentation study · Tata Memorial Hospital
Measured impact
Study-specific results for correctness and documentation time.
AE REPORTING CORRECTNESS
94.3%
Medical professional
76.2%
Foster
94.3%
+18.1 percentage points
Source: AE reporting study · Status: under review
LOWER DOCUMENTATION TIME
79%
Manual workflow
6 min
Foster
1.28 min
Source: Ambient documentation study · ESMO AI & Digital Oncology 2025
OBSERVED HALLUCINATIONS
0
300 evaluated encounters
Source: Ambient documentation study · Tata Memorial Hospital
Your data, protected
Your data, protected
Your data, protected
Your data, protected
Designed for sensitive clinical records and controlled review workflows.
Designed for sensitive clinical records and controlled review workflows.
Never used for model training
Foster does not use your patient records for model training.
Never used for model training
Foster does not use your patient records for model training.
Private and access-controlled
Confidential information remains private and access-controlled.
Private and access-controlled
Confidential information remains private and access-controlled.
Encrypted in transit & at rest
Your data is encrypted in transit and at rest.
Encrypted in transit & at rest
Your data is encrypted in transit and at rest.
COMMON
QUERIES
ANSWERED
What can Foster help our research team with?
Which record formats can we use?
Can we use our own study forms and protocols?
How are generated outputs checked?
How is patient data protected?
Does Foster also support clinical documentation?
COMMON
QUERIES
ANSWERED
What can Foster help our research team with?
Which record formats can we use?
Can we use our own study forms and protocols?
How are generated outputs checked?
How is patient data protected?
Does Foster also support clinical documentation?
What can Foster help our research team with?
Which record formats can we use?
Can we use our own study forms and protocols?
How are generated outputs checked?
How is patient data protected?
Does Foster also support clinical documentation?
COMMON QUERIES
ANSWERED
COMMON QUERIES
ANSWERED
What can Foster help our research team with?
Which record formats can we use?
Can we use our own study forms and protocols?
How are generated outputs checked?
How is patient data protected?
Does Foster also support clinical documentation?
AUTOMATE YOUR
NEXT CLINICAL STUDY
WITH FOSTER
Tell us about your study and the outputs your team needs.
AUTOMATE YOUR
NEXT CLINICAL STUDY
WITH FOSTER
Tell us about your study and the outputs your team needs.
AUTOMATE YOUR
NEXT CLINICAL STUDY
WITH FOSTER
Tell us about your study and the outputs your team needs.