Built on data from

FDAFDA
ClinicalTrials.govClinicalTrials.gov
PubMedPubMed
SEC EDGARSEC EDGAR
CMSCMS
NICENICE
HASHAS
G-BAG-BA
AIFAAIFA
FDAFDA
ClinicalTrials.govClinicalTrials.gov
PubMedPubMed
SEC EDGARSEC EDGAR
CMSCMS
NICENICE
HASHAS
G-BAG-BA
AIFAAIFA
FDAFDA
ClinicalTrials.govClinicalTrials.gov
PubMedPubMed
SEC EDGARSEC EDGAR
CMSCMS
NICENICE
HASHAS
G-BAG-BA
AIFAAIFA

How PE Teams Use Our Reports

Pre-LOI Screening

Rapid clinical and competitive landscape overviews to qualify or disqualify targets before committing resources to full diligence.

Confirmatory Due Diligence

Deep-dive reports covering regulatory pathway risk, clinical differentiation, and commercial potential to support IC memos.

Portfolio Monitoring Briefs

Event-triggered briefs when something moves: a competitor's poster at ASCO, an FDA complete response letter, a pivotal readout. 1-5 page actionable summaries delivered within 48 hours, so your team is never caught off guard.

Value Creation Planning

Evidence-based commercial strategy inputs for portfolio companies, including market access analysis, payer landscape mapping, and pricing benchmarks.

How It Works

From scoping call to board-ready deliverable in under two weeks.

Step 130 min call

Tell us what you need

Share your therapeutic area, target asset, and key business objective.

Step 25–10 business days

We build your report

Our analysts synthesize data from FDA filings, clinical trial data, press releases, and more, all into a structured intelligence brief.

Step 3

You make better decisions

Receive a polished, board-ready report with curated intelligence, underlying source data, and an AI assistant to interact with the data.

Every report is reviewed and verified by a domain expert

Our team carries deep biotech and pharma industry experience. No AI-generated filler. Every finding is reviewed, sourced, and cited.

Simple, Transparent Pricing

Choose the engagement model that fits your workflow.

Book a Call to Scope Your Report

No commitment required. We'll scope and quote on the call.

What You Get

Deep Dive

Comprehensive reports

Board-ready intelligence reports on competitive landscapes, regulatory assessments, and funding activity. Custom-scoped to your exact business question. Access to all underlying source data with LLM chat also provided.

10–40 pages

Length

5–10 business days

Delivery

Fully cited

Sources

Monitoring Briefs

Periodic & event-triggered updates

An emerging asset has early readout data at a conference. An FDA advisory committee votes unexpectedly. We deliver a concise, sourced brief so you can act immediately.

1–5 pages

Length

Within 48 hours

Delivery

Conferences, regulatory announcements

Triggers

Why choose Inflection Labs?

Turnaround

Inflection Labs

5-10 business days

DIY + AI

Minutes, but needs heavy QA

Big-4

6–12 weeks

In-House

Weeks to ramp up

Biopharma depth

Inflection Labs

Deep. Clinical, regulatory, commercial

DIY + AI

Surface-level, highly prone to hallucination

Big-4

Deep but specialized and narrow

In-House

Depends on hire

Cost

Inflection Labs

From $5K

DIY + AI

Low tool cost, high time cost

Big-4

$50K–$200K+

In-House

$150K+/yr salary

Data sources

Inflection Labs

FDA, CT.gov, PubMed, SEC, HTAs, Patent Repos, Conference Repos

DIY + AI

Public web + LLM training data

Big-4

Interviews + public data

In-House

Varies

Exec Team & Board-ready output

Inflection Labs

Yes. Polished & cited, with easily traceable source data

DIY + AI

Needs extensive editing & fact-checking

Big-4

Yes, but outputs lack adapability

In-House

Varies

Scalability

Inflection Labs

On-demand, any volume

DIY + AI

Fast but inconsistent quality

Big-4

Per project

In-House

Limited by headcount

Frequently Asked Questions

Ready to get started?

Book a 30-minute scoping call, or tell us what you need and we'll get back to you within 24 hours.

Book a Call

We typically respond within one business day. Your information is confidential and will not be shared.