Veeva MedInquiry logo

Veeva MedInquiry

by Veeva Systemsveeva.com
VISIT OFFICIAL WEBSITE →

OVERVIEW

A modern, cloud-based application for end-to-end management, fulfillment, and compliance of medical information requests in the life sciences industry.

Veeva MedInquiry is a core application within the Veeva Medical suite, built on the Veeva Vault platform, designed to streamline the entire lifecycle of medical information requests. It provides a centralized, compliant, and efficient solution for pharmaceutical, biotech, and medtech companies to manage inquiries from intake to fulfillment.

Product Overview and Key Benefits

MedInquiry serves as a single source of truth for all medical information requests, centralizing inquiries across products and geographies. This centralization ensures faster, more accurate inquiry response and drives efficiency by eliminating siloed systems and automating manual tasks. It is specifically designed for the highly regulated life sciences industry, ensuring all responses are constructed using approved, current content and maintaining compliance with global standards.

Main Features and Capabilities

  • Centralized Case Intake: Automatically receives and tracks inquiries from various channels, including a dedicated user interface, automated email ingestion, inbound telephony, live chat integration, and Veeva CRM.
  • Comprehensive Case Management: Manages the full lifecycle of an inquiry, including case assignment, contact management (integrating with Veeva OpenData and Network), and defining Service Level Agreements (SLAs).
  • Automated Response Generation: Detects Frequently Asked Questions (FAQs) and automatically creates response packages, including an email, cover letter, and approved content from the Vault Medical Library.
  • Controlled Content Distribution: Fulfills inquiries directly from Vault by sending response packages via email or a secure link, which controls document access and expiration to ensure content is always current and approved.
  • Adverse Event & Product Quality Complaint Capture: Enables the capture of data related to adverse events (AE) or product quality complaints (PQC) as part of a medical inquiry case and transfers this data to the appropriate safety/quality systems (e.g., Veeva Vault Safety, Veeva Vault Quality).
  • Reporting and Insights: Provides a full suite of Vault reporting and dashboards to gain insights into medical information trends and drive new content creation.

Target Users and Use Cases

Target Users: Medical Information teams, Medical Affairs professionals, Contact Center Agents, and Compliance/Quality personnel within Life Sciences organizations.

Use Cases:

  • Managing high-volume, global medical information requests.
  • Ensuring fast, consistent, and compliant responses to Health Care Professionals (HCPs) and consumers.
  • Automating the creation and distribution of approved scientific response packages.
  • Connecting medical inquiry data with safety and quality systems for seamless adverse event reporting.

RATING & STATS

Customers
60+
Founded
2007

KEY FEATURES

  • Centralized Case Intake (Email, Phone, CRM)
  • Automated Response Generation (FAQ/Standard Responses)
  • Controlled Content Distribution (Secure Link/Email)
  • Integration with Veeva CRM, Safety, and Quality
  • Adverse Event & Product Quality Complaint Capture
  • Compliance and Audit Trail Management
  • Case Contact Management (Veeva OpenData/Network)
  • Reporting and Dashboards

PRICING

Model: enterprise
Subscription-based, modular licensing model, typically priced per Vault application and per named user. Pricing is not publicly disclosed and is tailored to the enterprise customer's scale and modules deployed.

TECHNICAL DETAILS

Deployment: cloud, saas
Platforms: web
🔌 API Available

USE CASES

End-to-end Medical Information Request ManagementCompliant Scientific Content FulfillmentAdverse Event and Product Quality Complaint TriageGlobal Medical Affairs Operations Harmonization

INTEGRATIONS

Veeva CRMVeeva Vault MedCommsVeeva Vault SafetyVeeva Vault QualityVeeva OpenDataVeeva NetworkVault APIInbound Telephony/Live Chat

COMPLIANCE & SECURITY

Compliance:
ISO 27001ISO 27018SOC2 Type IIFDA 21 CFR Part 11 ComplianceGxP Compliance
Security Features:
  • 🔒Role-Based Access Control (RBAC)
  • 🔒Audit Trails
  • 🔒Encryption (Data in Transit and At Rest)
  • 🔒Secure Link Fulfillment

SUPPORT & IMPLEMENTATION

Support: email, phone, 24/7 support, dedicated account manager
Implementation Time: 1-3 months
Target Company Size: medium, enterprise
TRAINING AVAILABLE

PROS & CONS

✓ Pros:
  • +Ensures regulatory compliance (21 CFR Part 11, GxP) by using a single source of truth for content.
  • +Seamless and deep integration with the broader Veeva Vault and CRM ecosystem.
  • +Significant automation of case intake and response package generation, leading to faster response times.
  • +Centralized global platform for harmonizing medical information processes across regions.
✗ Cons:
  • -High enterprise cost and non-public pricing (inferred from Veeva's model).
  • -Steep learning curve and complexity typical of highly specialized enterprise Vault applications.
  • -Requires significant implementation and configuration time.

ABOUT VEEVA SYSTEMS

Other software by Veeva Systems:
Veeva QMS (Procurement & Vendor ManagementSupplier quality management)
Veeva Submissions (Regulatory Affairs & ComplianceSubmission lifecycle tracking)
Veeva Vault PromoMats (Marketing & Commercial OperationsPharma marketing automation (compliant))
Veeva Vault RIM (Regulatory Affairs & ComplianceRegulatory Information Management (RIM))