Real-World Evidence & Drug Safety

The Post-Marketing Surveillance & Pharmacovigilance Platform

WH PMS enables pharmaceutical companies to run real-world evidence studies, monitor drug safety, track adverse events, and manage field operations — all in one secure, multi-tenant platform.

Request a Proposal
10
User Roles
Multi
Tenant
RWE
Studies
GVP
Compliant
WH PMS
A complete pharmacovigilance ecosystem
Built for post-market drug surveillance with integrated data collection, monitoring, and analytics.

Patient Enrollment & Tracking

Enroll patients, capture demographics and medical history, and track multi-visit timelines from baseline through every follow-up visit.

EnrollmentPatient CardsFollow-upsHistory

Adverse Event Reporting

Document adverse events with severity classification, serious AE flagging, recovery tracking, actions taken, and outcome recording.

AE ReportingSeveritySerious AEOutcomes

Clinical Assessment

Baseline and follow-up visit documentation, efficacy assessments, treatment response monitoring, vital signs, and lab results.

BaselineEfficacyVitalsLab Results

Field Operations & Visits

Medical reps log physician visits, key messages, discussion points, and field reports with feedback and follow-up flagging.

Physician VisitsField ReportsFeedbackTracking

Product & Study Management

Configure pharmaceutical products with codes, active ingredients, and dosages. Set up PMS and pharmacovigilance study protocols.

ProductsStudy TypesProtocolsMulti-Product

Targets & KPI Tracking

Set monthly and yearly targets for medical reps, track visit and prescription goals, and monitor achievement against territory objectives.

TargetsKPIsGoalsTerritory

Analytics & Dashboards

Product-specific study dashboards, enrollment statistics, completion rates, team performance rankings, and trend analysis.

DashboardsEnrollmentRankingsTrends

Reporting & Export

Individual patient PDF cards with custom branding, bulk Excel/CSV exports, executive summaries, and regulatory submission support.

PDF CardsExcel/CSVExecutiveRegulatory

Multi-Company Management

Multi-tenant architecture with company branding, custom themes, email domain patterns, and product assignment per pharmaceutical company.

Multi-TenantBrandingThemesCompanies

User & Role Management

Role-based access for 10 distinct user types, bulk import/export, online user monitoring, audit logs, and approval workflows.

RBACAudit LogsOnline UsersWorkflows

Patient Self-Reporting

Patients log daily symptoms, severity, side effects, and medication compliance, with secure messaging to their physicians.

Symptom LogsComplianceMessagingQoL

Notifications & Training

System-wide announcements, brand manager broadcasts, performance feedback, and a role-based tutorial video library.

AnnouncementsBroadcastsTutorialsAlerts
Specialized tools for every stakeholder
From physicians collecting data to brand managers overseeing teams — each role has a tailored interface.
Platform-wide configuration and settings
Manage pharmaceutical companies and branding
Configure products and study types
User management across all companies
Platform-wide analytics and reporting
Audit logs and online user monitoring
Patient enrollment and registration
Baseline and follow-up visit documentation
Adverse event reporting and classification
Efficacy and treatment response tracking
Export patient cards (PDF)
Personal enrollment dashboard
Physician visit management and scheduling
Field report submission with attachments
Product-specific study dashboards
Territory coverage and mapping
Personal KPI and target tracking
Notifications from brand managers
Manage and assign medical reps
Assign physicians to reps by territory
Team performance analytics and rankings
Set targets and track goal progress
Review and approve field reports
Executive reporting and broadcasts
Personal health profile management
Daily symptom and severity logging
Medication compliance tracking
Secure messaging with physicians
Treatment timeline and reminders
Secure & CompliantRBAC, encryption & audit trails
Multi-TenantUnlimited companies & studies
PharmacovigilanceAdverse event & safety monitoring
Real-World EvidenceData-driven study insights

Ready to strengthen your drug safety program?

See WH PMS in action or request a tailored proposal for your organization.