Pfizer
Novartis
AstraZeneca
Roche
Johnson & Johnson
Merck
AbbVie
Bristol-Myers
Eli Lilly
Sanofi
GSK
Bayer
Amgen
Gilead
Biogen
Pfizer
Novartis
AstraZeneca
Roche
Johnson & Johnson
Merck
AbbVie
Bristol-Myers
Eli Lilly
Sanofi
GSK
Bayer
Amgen
Gilead
Biogen
Pharmaceutical Training Engine

Your Reps Launch
in 14 Days.
Not 14 Weeks.

Compound drills drug interactions, compliance protocols, and formulary updates into your reps before their first hospital call — with audit-ready certification records built in.

14
Days to field-ready
40+
Territories in parallel
100%
Audit-ready proof
app.compound.io/dashboard/rep/training
Rep Dashboard — Jordan Nakamura
Oncology Product Launch · Cohort 04
Completion
73%
0%73% complete100%
Active Quiz

A physician prescribes Venetoclax with strong CYP3A inhibitors. What dose adjustment is required per current formulary guidelines?

Reduce by 75%
No adjustment needed
Contraindicated
Reduce by 50%
Session Log — Today
Drug Interactions — Module 4
09:14 AM94%PASS
Formulary Tier Classification
09:41 AM88%PASS
Off-Label Compliance Brief
10:02 AM91%PASS
Adverse Event Reporting SOP
In ProgressACTIVE
Technical Specifications
Rev. 2026.02
01
Spec 01: Onboarding Speed

14 Days to Field-Ready Certification

14
Days average to full certification
  • Adaptive learning paths that compress 11 weeks of classroom content into structured daily modules.
  • Automated cohort scheduling — provision 40 territories simultaneously from one admin dashboard.
  • Daily progress nudges sent via email and SMS keep completion rates above 94%.
Onboarding Timeline — Cohort 04
Day 1
Account provisioned + cohort assigned
Day 3
Core drug interaction modules completed
Day 7
Compliance certification exam passed
Day 10
Formulary deep-dive + role-play scenarios
Day 14
Field-ready status granted ✓
Industry avg: 11 weeksCompound: 14 days
02
Spec 02: Content Library

6,400+ Modules. Updated Within 48 Hours of FDA Label Changes.

6,400+
Active training modules across 14 therapeutic areas
  • Drug interaction databases cross-referenced with current formulary tiers and payer restrictions.
  • Role-specific content tracks for Oncology, Cardiology, Neurology, and Rare Disease.
  • Every module maps to a compliance checkpoint — nothing slips through for auditors.
Content Library6,400+ modules
Drug Interactions2,840
Formulary Updates1,240
Compliance Protocols890
Adverse Event Reporting540
Off-Label Guidelines320
Updated within 48h of FDA label changes
03
Spec 03: Compliance Tracking

Audit-Ready Proof. Every Rep. Every Module. Exportable in 60 Seconds.

100%
Certification traceability per rep, per module
  • Timestamped completion records with quiz scores, attempt counts, and session duration.
  • One-click export to CSV, PDF, or direct API pull for your compliance management system.
  • Built to satisfy FDA 21 CFR Part 11, PDMA, and internal SOX audit requirements.
Compliance Audit Export
FDA Ready
Jordan Nakamura
Oncology L1
02/14/26CERTIFIED
Priya Mehta
Cardio L2
02/15/26CERTIFIED
Marcus Webb
Oncology L1
02/15/26CERTIFIED
Sasha Kowalski
Neuro L1
02/16/26CERTIFIED
Devon Okafor
Cardio L1
02/17/26IN REVIEW
Export: CSV · PDF · API4/5 certified
04
Spec 04: Integrations

Plugs Into Veeva, Salesforce, and Your Existing LMS in One Sprint.

<1 day
Average integration time with your existing stack
  • Native connectors for Veeva CRM, Salesforce Health Cloud, Cornerstone, and SAP SuccessFactors.
  • SCORM 2004 and xAPI compliance for any LMS that speaks standards.
  • REST API with full Swagger docs — your IT team ships the integration before your kickoff call ends.
Integration HubREST API + SCORM 2004
Veeva CRM
CRMConnected
Salesforce Health
CRMConnected
Cornerstone LMS
LMSConnected
SAP SuccessFactors
HRISConnected
Workday Learning
LMSConnected
Custom SCORM
LMSAvailable
SSO · SAML 2.0 · SOC 2 Type II certified
Compound — 14-Day Rep Certification Platform
Primary Path

Request Your Pilot

Get a 14-day pilot configured for your therapeutic area, rep count, and compliance requirements. We provision within 24 hours.

No credit card. Provisioned within 24 hours. Cancel anytime.

Secondary Path

Download the Spec Sheet

Not ready to pilot? Get the full technical specification PDF — module architecture, integration docs, compliance framework, and pricing tiers.

What's inside the spec sheet
14-page technical architecture overview
Full integration compatibility matrix (Veeva, Salesforce, 12+ LMS)
Compliance framework mapped to FDA 21 CFR Part 11
Pricing tiers for 50 to 5,000+ reps
Case study: 340-rep oncology launch in 12 days