For Healthcare Private Equity

Diligence Every Deal Across Your Pipeline.

IC-grade clinical, regulatory, and manufacturing diligence on each target — from an automated Quick Screen for triage to Diligence and M&A Reports reviewed by a physician and a biomedical engineer. Firms screening at volume can license Vantage through Enterprise, priced to the portfolio. Factual claims are cited to their sources.

Talk to Arvind Ravinutala, MD Enterprise License — Priced to Your Portfolio See a Sample Evaluation
A·A
Vantage full reports are reviewed by Arvind Ravinutala, MD (practicing physician, P&T Committee Chair) and Aswini Ravinutala, BME (biomedical engineer, 10+ years in medical devices). The Quick Screen is automated. Specialist consultation is available when an engagement needs it.

I am a:

Founder Investor/VC PE Firm Corporate Acquirer University/TTO Incubator

Screening a Pipeline

Screen Each Target on the Same Six Signals

Run a Quick Screen on each company in your pipeline: six independent signals per company, each linked to its source records, with no composite score and no ranking verdict.

Pipeline screening

Competitive Advantage

Platform-Grade Intelligence at Speed & Scale

Big 4 Consulting

  • ● Higher cost for platform DD
  • ● Timelines often measured in weeks
  • ● Medtech depth varies by team
  • Limited medtech focus

Boutique Advisors

  • ● Deep domain expertise
  • ● Frameworks vary by advisor
  • ● Depth depends on the individual
  • Limited portfolio comparison

Vantage

  • ✓ Purpose-built for medtech
  • ✓ Comparables from 3,900+ companies across 34 public sources
  • ✓ Eight diligence domains
  • Physician + biomedical engineer review · factual claims cited to their sources, independent of deal parties

Faster and less expensive than a traditional analyst engagement, with sources you can check.

What We Find

Six Risk Areas PE Diligence Reads

Six of the areas a full report reads.

8

Diligence domains per full report

3,900+

Companies in our substrate

34

Public data sources

MD + BME

Review on full reports

Clinical Adoption

Will physicians change workflow? The report reads the adoption questions a financial review is not built to ask.

Manufacturing

Manufacturing, quality and supplier questions, read from recalls, FDA records and the materials you provide.

Regulatory Pathway

Predicate and pathway questions, read against FDA's record. A misjudged pathway can add months and material cost.

Reimbursement

Devices with unclear payer pathways can stall after FDA authorization. The report reads coding, coverage and payment records.

Comparable Companies

Comparable companies drawn from a substrate of 3,900+ biomedical companies and 4.7 million public records.

Payer Concentration

Reliance on a single payer is a concentration risk. The report shows where coverage decisions sit in the public record.

Pricing

Enter Per Deal. Scale to an Enterprise License.

Per-deal reports are the entry point. Firms screening at volume can license Vantage through Enterprise, with a scoped annual report allowance priced to the portfolio.

Platform • Tier 1

Quick Screen

$5,000
Automated • 24 hours after a complete intake
  • Six independent signals
  • Each linked to its source records
  • No composite score or verdict
  • Fee credits toward a full report
Ideal for: Pipeline screening, initial deal filtering
Platform • Tier 2

Diligence Report

$20,000
Physician and engineer review • 48 hours
  • Eight domains with cohort comparables
  • Competitive positioning & market context
  • Claims cited to their source records
  • Debrief with Arvind Ravinutala, MD
Ideal for: Pre-LOI evaluation, IC presentation, finalist validation
Report • Tier 3

M&A Report

$25,000
48 hours • 60-minute strategy session
  • Everything in the Diligence Report
  • Integration risk
  • Reference-contact review
  • For platform and bolt-on decisions
Ideal for: Post-LOI, platform builds, bolt-on acquisitions, IC sign-off

Typical PE workflow: Start with a Quick Screen across the pipeline, commission a Diligence Report on finalists, and use the M&A Report for platform or bolt-on acquisitions. Firms screening at volume can license Vantage through Enterprise, priced to the portfolio. Contact us for a scoped proposal.

Enterprise: a scoped annual Quick Screen and Diligence Report allowance, priced to your portfolio. Per deal: Quick Screen $5,000 · Diligence Report $20,000 · M&A Report $25,000.

Request a custom program →

What's the Cost of Not Knowing?

A single missed clinical, manufacturing or reimbursement question can cost far more than the diligence that would have surfaced it.

Average Deal Size
Report Cost
$20,000
Diligence Report
Cost as % of Deal
0.133%
of the deal

Deal Integration

Vantage in Your Deal Lifecycle

From deal sourcing through the investment committee

1

Deal Sourcing

Quick Screens across inbound deals

2

Initial Screen

Rapid triage on target profile and strategic fit

3

Deep Diligence

Diligence Report on finalists

4

IC Review

Diligence findings in front of the IC

5

Platform & Add-ons

M&A Report on platform or bolt-on targets

How we'd diligence a platform

Three integration risks we test for — applied to public outcomes

Each card is a public retrospective, not a private case. The point is to show the framework: what the public record showed, and the questions it raised.

See all public retrospectives → Discuss a platform DD

These are public retrospectives, not client engagements.

Enterprise License for PE Portfolios

A scoped annual allowance of Quick Screens and Diligence Reports across your platform and add-ons, priced to your portfolio. Factual claims are cited to their sources, drawn from our proprietary multi-source substrate.

Talk to Arvind Ravinutala, MD →

Diligence Your Next Deal — or License the Whole Portfolio

Enter per deal with a Quick Screen or Diligence Report, or talk to Arvind Ravinutala, MD, about an Enterprise license priced to your portfolio.

Talk to Arvind Ravinutala, MD See the Quick Screen — $5,000 Diligence Report — $20,000

Free Download: Red Flags Guide

10 regulatory, clinical, and commercial red flags to check before a healthcare deal — written by Arvind Ravinutala, MD and Aswini Ravinutala, BME.

Download the Guide

No email required. No paywall.

See the framework on a real outcome

Before you go — see the framework applied to Exactech’s device recalls and 2024 bankruptcy, from the public record. Read the retrospective →