Biopharma R&D
Own your trial budgets, from site contract to invoice
Site budgets from your own benchmarks, every invoice against plan and spend you can forecast, for clinical operations and R&D finance.

Biopharma R&D
Own your trial budgets, from site contract to invoice
Site budgets from your own benchmarks, every invoice against plan and spend you can forecast, for clinical operations and R&D finance.

Biopharma R&D
Own your trial budgets, from site contract to invoice
Site budgets from your own benchmarks, every invoice against plan and spend you can forecast, for clinical operations and R&D finance.

A week in R&D budgets
Where an R&D budget week goes
Site budgets, invoices and scenarios still run on last year’s spreadsheet in most clinical operations teams.
A week in R&D budgets
Where an R&D budget week goes
Site budgets, invoices and scenarios still run on last year’s spreadsheet in most clinical operations teams.
A week in R&D budgets
Where an R&D budget week goes
Site budgets, invoices and scenarios still run on last year’s spreadsheet in most clinical operations teams.
Industry data
Every change reprices the trial. Amendments are the rule, not the exception.
Amendments
3.3
substantial amendments per protocol, on average
Phase III
82%
of Phase III protocols need at least one
Time
260
days from sign-off to the last ethics approval
Tufts CSDD amendment study: Getz KA et al., Therapeutic Innovation & Regulatory Science, 2024; Applied Clinical Trials, December 2023.
Industry data
Every change reprices the trial. Amendments are the rule, not the exception.
Amendments
3.3
substantial amendments per protocol, on average
Phase III
82%
of Phase III protocols need at least one
Time
260
days from sign-off to the last ethics approval
Tufts CSDD amendment study: Getz KA et al., Therapeutic Innovation & Regulatory Science, 2024; Applied Clinical Trials, December 2023.
Industry data
Every change reprices the trial. Amendments are the rule, not the exception.
Amendments
3.3
substantial amendments per protocol, on average
Phase III
82%
of Phase III protocols need at least one
Time
260
days from sign-off to the last ethics approval
Tufts CSDD amendment study: Getz KA et al., Therapeutic Innovation & Regulatory Science, 2024; Applied Clinical Trials, December 2023.
One system of record for your trial spend
Clinical trial budget management next to your CTMS, ERP and payment provider. Not replacing your systems. Orchestrating them.
From site contract to month-end accruals
Site budgets with versions and an awarded version, priced from your own benchmarks, with CRO and vendor budgets beside them; every invoice recorded against them, flagged when off budget, with month-end accruals.




An enrollment change, priced in the meeting
Scenario planning prices more patients, a delay or one more site in seconds; spend projection turns it into R&D spend by quarter for the business plan and latest estimates.
A Decision Cockpit for the R&D portfolio
Every study shows its forecast at end, burn vs. progress and health status with alerts; leadership compares business units and cost per patient, with unlimited read-only viewers.


One system of record for your trial spend
Clinical trial budget management next to your CTMS, ERP and payment provider. Not replacing your systems. Orchestrating them.
From site contract to month-end accruals
Site budgets with versions and an awarded version, priced from your own benchmarks, with CRO and vendor budgets beside them; every invoice recorded against them, flagged when off budget, with month-end accruals.




An enrollment change, priced in the meeting
Scenario planning prices more patients, a delay or one more site in seconds; spend projection turns it into R&D spend by quarter for the business plan and latest estimates.
A Decision Cockpit for the R&D portfolio
Every study shows its forecast at end, burn vs. progress and health status with alerts; leadership compares business units and cost per patient, with unlimited read-only viewers.


One system of record for your trial spend
Clinical trial budget management next to your CTMS, ERP and payment provider. Not replacing your systems. Orchestrating them.
From site contract to month-end accruals
Site budgets with versions and an awarded version, priced from your own benchmarks, with CRO and vendor budgets beside them; every invoice recorded against them, flagged when off budget, with month-end accruals.




An enrollment change, priced in the meeting
Scenario planning prices more patients, a delay or one more site in seconds; spend projection turns it into R&D spend by quarter for the business plan and latest estimates.
A Decision Cockpit for the R&D portfolio
Every study shows its forecast at end, burn vs. progress and health status with alerts; leadership compares business units and cost per patient, with unlimited read-only viewers.


Ready for R&D finance, procurement and IT
The answers a biopharma review asks for, before the first study goes live.
Business Units, One Instance
Several business units in one instance, separated by roles and compared in reports.
Single Sign-On
Entra ID, Okta or Google via OpenID Connect, plus MFA and IP allow-listing.
Germany, EU or US
Hosted where your setup requires, encrypted in transit and at rest.
Rollout to Your Scope
Self-service study setup; migration, training and hypercare as your scope needs.
Audit-Ready
Every change and every export logged; GDPR-compliant, with 21 CFR Part 11 readiness.
Your Data, Your Exit
Complete CSV export at any time; DPA, SLA and exit clause in the agreement.
Ready for R&D finance, procurement and IT
The answers a biopharma review asks for, before the first study goes live.
Business Units, One Instance
Several business units in one instance, separated by roles and compared in reports.
Single Sign-On
Entra ID, Okta or Google via OpenID Connect, plus MFA and IP allow-listing.
Germany, EU or US
Hosted where your setup requires, encrypted in transit and at rest.
Rollout to Your Scope
Self-service study setup; migration, training and hypercare as your scope needs.
Audit-Ready
Every change and every export logged; GDPR-compliant, with 21 CFR Part 11 readiness.
Your Data, Your Exit
Complete CSV export at any time; DPA, SLA and exit clause in the agreement.
Ready for R&D finance, procurement and IT
The answers a biopharma review asks for, before the first study goes live.
Business Units, One Instance
Several business units in one instance, separated by roles and compared in reports.
Single Sign-On
Entra ID, Okta or Google via OpenID Connect, plus MFA and IP allow-listing.
Germany, EU or US
Hosted where your setup requires, encrypted in transit and at rest.
Rollout to Your Scope
Self-service study setup; migration, training and hypercare as your scope needs.
Audit-Ready
Every change and every export logged; GDPR-compliant, with 21 CFR Part 11 readiness.
Your Data, Your Exit
Complete CSV export at any time; DPA, SLA and exit clause in the agreement.
Questions from biopharma R&D teams
Short answers for clinical operations, R&D finance, procurement and IT.
What is clinical trial financial management?
Planning, tracking and forecasting what a clinical trial costs: site budgets, invoices, accruals and forecasts in one system. The Sponsor Suite does this for biopharma R&D, for pharma and biotech sponsors alike, next to your CTMS, ERP and payment provider.
Does it cover site budgets and investigator grants?
Who uses the Sponsor Suite?
Can R&D finance plan R&D spend with it?
Can several business units share one instance?
How long does a rollout take?
Questions from biopharma R&D teams
Short answers for clinical operations, R&D finance, procurement and IT.
What is clinical trial financial management?
Planning, tracking and forecasting what a clinical trial costs: site budgets, invoices, accruals and forecasts in one system. The Sponsor Suite does this for biopharma R&D, for pharma and biotech sponsors alike, next to your CTMS, ERP and payment provider.
Does it cover site budgets and investigator grants?
Who uses the Sponsor Suite?
Can R&D finance plan R&D spend with it?
Can several business units share one instance?
How long does a rollout take?
Questions from biopharma R&D teams
Short answers for clinical operations, R&D finance, procurement and IT.
What is clinical trial financial management?
Planning, tracking and forecasting what a clinical trial costs: site budgets, invoices, accruals and forecasts in one system. The Sponsor Suite does this for biopharma R&D, for pharma and biotech sponsors alike, next to your CTMS, ERP and payment provider.
Does it cover site budgets and investigator grants?
Who uses the Sponsor Suite?
Can R&D finance plan R&D spend with it?
Can several business units share one instance?
How long does a rollout take?
Bring one site budget and one question
Start with a 30-minute call about your trials — the demo that follows builds a site budget, records an invoice and prices your open scenario.
Bring one site budget and one question
Start with a 30-minute call about your trials — the demo that follows builds a site budget, records an invoice and prices your open scenario.
Bring one site budget and one question
Start with a 30-minute call about your trials — the demo that follows builds a site budget, records an invoice and prices your open scenario.