Capabilities
Product depth built for how pharma teams actually decide.
From molecule intelligence and risk scoring to NPV/eNPV, materials readiness, and audit-ready governance, every capability stays connected to the same asset record.
Where PortiVix leads
Five capabilities generic tools were not built for.
- 01
Molecule Intelligence
A governed asset record from public FDA data import through enrichment, phase gates, and snapshots.
- 02
Risk Intelligence
PTRS, Business, IP, API/Supply, and KSM scoring separated from delivery risk and issues.
- 03
NPV / eNPV
Risk-adjusted value connected to probability, assumptions, and actuals.
- 04
Audit-ready governance
Traceability created as work happens, actor identity, change history, checksum, export.
- 05
Pharma project execution
Milestone → task → subtask, dependencies, critical path, risks, and issues.
Molecule intelligence
Build and manage every asset record from one governed source of truth.
Create molecules manually or use the Portfolio Builder to start from public FDA datasets, then enrich each asset with commercial assumptions, phase gates, patent fields, risks, financials, materials, documents, and snapshots.
Portfolio Builder
Portfolio Builder
Drug search across public FDA data and Orange Book-style workflows to start a molecule record.
Raw source payload stored for imported records
Manual enrichment after creation
Public data gives a starting point; your teams validate and enrich
Shown: Molecule record, header
Dosage form
Molecule profile
A complete asset profile across pharma, patent, and lifecycle fields.
Dosage formroutestrengthcontainerstoragebrandShown: Details, Dosage form and Strengths
Filing category
Molecule profile
A complete asset profile across pharma, patent, and lifecycle fields.
Filing categorymarketdevelopment modelShown: Details, Filing route and Portfolio
Patent/IP
Molecule profile
A complete asset profile across pharma, patent, and lifecycle fields.
Patent/IP: DS, DP, and AoP expiry dates
Shown: Patents
Phase timelines
Molecule profile
A complete asset profile across pharma, patent, and lifecycle fields.
Phase timelinesbaselinessnapshotshold/resume lifecycletask boardsShown: Stage progress
Portfolio governance
Leadership visibility without a briefing-pack dependency.
Live visibility into molecule status, project progress, phase movement, risks, issues, resources, and financial signals across the pipeline.

- Portfolio Command Centre
- Portfolio Trends
- Programme-level PMO Governance Dashboard
- Portfolio and project Gantt views
- Access rules by user, role, and discovery mode
- Named owner accountability
Governed execution
Milestone to activity, with critical path, risks, and issues in one plan.
Structured project plans move pharma teams from informal coordination to accountable execution: Project → Milestone → Task → SubTask, with dependencies, critical path, an interactive Gantt, a project risk register, and an issue tracker.

Plan structure
- Milestones, tasks, subtasks, activities
- Dependencies: FS, SS, FF, SF with lag days
- Interactive Gantt and critical path indicators
- Template lock mechanics for governed plans
Risk, issues & sign-off
- Project risk register: probability, impact, owner, mitigation, residual risk
- Issue tracker: blockers, deviations, change requests, escalation
- Task approvals, pending queue, rejection reasons, sign-off
- Comments, @mentions, documents, activity feed, audit trail
Risk and issue control
Know where risk sits before it becomes a missed milestone or bad capital decision.
PortiVix separates molecule-level decision risk from project-level delivery risk and active issues, giving leadership and PMO teams a clearer view of what could go wrong and what already has.
- PTRSProbability of technical and regulatory success at phase gates.
- Business RiskCommercial viability, competition intensity, and strategic fit.
- IP RiskFreedom-to-operate, patent vulnerability, and patent cliff exposure.
- API / Supply RiskSupplier concentration, lead time, country risk, and regulatory supply exposure.
- KSM RiskScoring and commentary.
- Project Risk RegisterProbability, impact, owner, mitigation, contingency, residual risk, review date, status.
- Issue TrackerBlockers, deviations, change requests, linked tasks, comments, and escalation.


NPV and eNPV
Connect capital decisions to molecule risk and execution reality.
Each molecule can carry a financial model with NPV and expected NPV, so leaders and finance teams understand value, probability, assumptions, and actuals in the same context as phase gates and risk. Try it: adjust the inputs and watch eNPV move.
- NPV (unrisked)
- $631m
- eNPV (risk-adjusted)
- $235m
Phase-gate signal Hold / re-baseline
Illustrative model. In PortiVix, eNPV connects to real assumptions, actuals, PTRS, and risk on each molecule.
Model inputs
- 01
API priceCOGSannual demandoverheadother costsinvestmentdiscount rateproject durationprobability of successstart year
Outputs & actuals
- 01NPV and eNPV for risk-adjusted prioritisation
- 02Annual cashflow actuals for comparison against the model
- 03What-if recalculation on save
Pharma decision flow
Molecule profile
commercial & patent fields
Shown: Molecule record, header and summary
Risk scoring
PTRS · IP · API · KSM
Shown: Molecule record, Risk profile
NPV / eNPV
risk-adjusted value
Shown: Molecule record, Value
Phase-gate decision
go / kill evidence
Shown: Molecule record, Gate 2 evidence
Audit record
attached as it happens
Shown: Audit Log, verified chain
Materials and supply chain
Bring material readiness into the same view as molecule and project decisions.
For API, formulation, and development teams, material and vendor readiness can decide whether timelines are real.

- DQ, SU, EB (exhibit batch), and Commercial quantity planning
- Material items: type, CAS number, UOM, contribution %
- Vendor records: unit price, budget, lead time, country of origin, markets
- Materials Dashboard for portfolio-level KPIs
- Version history for traceability
20+ reports and AI-assisted intelligence
Reports built around decisions, not around what happens to be available.
Strategic, monitoring, operational, and compliance reports with saved views, scheduled delivery, exports, and AI-assisted portfolio questions that respect user access permissions.
Strategic
- Portfolio Command Centre
- PMO Governance Dashboard
- Portfolio Trends
- My Dashboard
Monitoring / Control Tower
- Risk Control Tower
- Issue Control Tower
- Milestone Governance
- Resource Utilisation
Operational
- Project Summary
- Task Completion
- Workstream Progress
- Milestone Tracking
- Project Burndown
- Employee Utilisation
Data & Compliance
- Risk Registry
- Issue Registry
- Portfolio Health
- Audit & Compliance
AI Assistant
Ask portfolio questions such as at-risk molecules, top eNPV opportunities, and portfolio health summaries. AI access is scoped by RBAC and audited through tools-used tracking, and it only uses the data available to the authenticated user.
Governance, audit & compliance
Evidence that exists before you need it.
Approval, phase, change, and audit records stay connected to the work as it happens, supporting regulated electronic-record readiness, including 21 CFR Part 11 readiness workflows, subject to customer validation.
Audit trail flow
Action
create · update · export
Event coverage & export
CreateupdatedeleteviewexportloginlogoutPermission changes, role assignments, password resets, and more
Shown: Events, Action column
Actor
identity · role · IP
What each record captures
Actor identityIP addressuser agentsession IDrolestimestampShown: Entry detail, User, Email and Source
Timestamp
session context
What each record captures
timestampShown: Events, Time column
Before / after state
change captured
What each record captures
Before/after state for changes
Shown: Entry detail, What changed
Checksum
integrity verification
What each record captures
Checksum verification for log integrity
Event coverage & export
Checksum verification endpoint for integrity checks
Shown: Entry detail, Integrity
Export
CSV for review
Event coverage & export
CSV export for audit and compliance review
Shown: Audit Log, Export log
See these capabilities mapped to your workflows.
We do not start with a generic demo. We map your portfolio, molecule, project, approval, reporting, and governance workflows first, then show how PortiVix would work for your organisation.
Or write to marketing@virtunx.com

