What you can use right now
Resource Library
Curated TransCelerate, ICH, FDA, EMA references for sponsors.
Trial Budget Calculator
Total trial estimation aligned to industry budget structures.
AVD original SOPs
Sponsor-level SOPs: pharmacovigilance, QMS, protocol development, regulatory submissions, CSR, CSV, sponsor oversight, audit & inspection.
What we are building for sponsors
Sponsor portal login
Authenticated logins for medical monitors, regulatory, operations, finance. Audit-logged access.
CRO oversight view
Visibility into CRO duties as defined in the Transfer of Obligations matrix. Performance scorecards. Deviation tracking.
Multi-study budget tracking
Roll-up across active studies. Compare planned vs actual. Identify variance drivers.
Regulatory submission view
Visibility into submission status, agency questions, and response timelines (informational; does not replace your eCTD system).
KRI / QTL dashboards
Quality Tolerance Limit monitoring with threshold-based alerts.
Site relationship view
See which sites are performing across multiple studies; data-informed site selection for future trials.
How sponsors actually use AVD today
CSR structural backbone
A medical writer uses the AVD CSR SOP as backbone for a Phase 2 CSR.
Pre-submission checklist
A regulatory lead uses the AVD Regulatory Submissions SOP as a pre-submission checklist.
QMS benchmarking
A QA director benchmarks their QMS against the AVD QMS framework.
Get started
Use the free resources today. For enterprise platform access, send us a message about your portfolio scope.