Whether you need expert pharmacovigilance consulting, complete operational support, or a validated cloud-based pharmacovigilance software platform, we offer flexible pricing models designed around your business size, product portfolio, regulatory requirements, and reporting volume.
Customized based on your requirements
Flexible plans with scalable features
Every organization has unique pharmacovigilance needs. Our consulting pricing is customized based on the scope of work, regulatory requirements, number of products, markets served, reporting volume, and project complexity.
Instead of fixed packages, we provide a detailed cost estimate after understanding your operational requirements.
Whether you are a startup with a few safety cases or a global pharmaceutical company managing thousands of adverse event reports, our subscription plans scale with your growth.
| Features |
Basic
For Small Scale Manufacturers to MAH Holders requiring mandatory PV Regulatory Compliance Digital Framework |
Prime
For Small to Mid Sized Companies looking for end-to-end PV Solutions along with Regulatory Compliance |
Enterprise
For MNCs looking for PV Solution for USA, Europe or Other Regulated Region and Clinical Research Organizations (CROs) |
|---|---|---|---|
| License | Single | Single | Multiple |
| Hosting | Cloud | Cloud | Cloud / On-Premises |
| Validity | Annual | Annual | Annual |
| Dedicated Web URL | ✓ | ✓ | ✓ |
| Multilingual ADR Reporting | ✓ | ✓ | ✓ |
| Initial Receipts (ICSR) / Year | 100 | 250 | 1000+ |
| Product Master | 250 Products | 500 Products | Unlimited |
| Product Leaflet | ✓ | ✓ | ✓ |
| Role Based Access (RBAC) | ✓ | ✓ | ✓ |
| Login with Central Admin | ✓ | ✓ | ✓ |
| Total Users | 4 | 7 | Variable |
| Admin Role | ✓ | ✓ | ✓ |
| Product Safety Associate | 1 | 2 | Variable |
| Medical In-Charge | 1 | 2 | Variable |
| Quality In-Charge | 1 | 2 | Variable |
| Storage | 500 MB | 1 GB | 10 GB |
| Data Backup | ✓ | ✓ | ✓ |
| Download Data | ✓ | ✓ | ✓ |
| Audit Trail (21 CFR Part 11) | ✓ | ✓ | ✓ |
| E2B(R3) XML Export | ✓ | ✓ | ✓ |
| IQ/OQ/PQ Documentation | Add-On | Add-On | Add-On |
| Electronic Signature | Add-On | Add-On | Add-On |
| Auto Regulatory Submission | Add-On | Add-On | Add-On |
| MedDRA Integration | x | x | Add-On |
| PSUR Reports | x | x | ✓ |
| Digital PSMF | x | x | ✓ |
| Risk Management Plan | x | x | ✓ |
| AI Reports & Analytics | x | x | ✓ |
| API Integration | x | x | ✓ |
| Support | Remote | Remote | Onsite |
No unnecessary enterprise costs.
Upgrade your subscription as your pharmacovigilance operations expand.
Transparent licensing and consulting costs.
Built for FDA, EMA, ICH E2B(R3), GVP, and 21 CFR Part 11 compliance.
Encrypted cloud infrastructure with comprehensive audit trails, backup, disaster recovery, and role-based security.
Yes. All plans are designed to scale. You can upgrade users, products, storage, or annual ICSR capacity at any time without losing your existing data.
Yes. Enterprise customers can choose annual subscription, multi-year licensing, or perpetual on-premise licensing based on commercial requirements.
Basic implementation is included with Professional plans and above. Enterprise projects may also include migration, validation, user training, and system integrations.
MedDRA integration is fully supported. The MedDRA subscription itself is obtained separately by customers in accordance with MSSO licensing requirements.
Yes. IQ, OQ, PQ documentation together with Computer System Validation (CSV) support is available for regulated organizations.
Yes. Schedule a personalized live demonstration with our product specialists to explore features, workflows, and compliance capabilities before making a decision.