Pharmacy Brokerage Services / Confidential Index / PBS-0417

Live sell-side mandate

A turnkey sterile facility that can't be rebuilt in a hurry.

A confidential opportunity to acquire a fully built-out cGMP 503B sterile compounding facility in Southern California — constructed 2015–2018, FDA-inspected in 2019, and offered turnkey. Replicating it would cost tens of millions and years of qualification. Identity and full detail are released to qualified buyers under a mutual non-disclosure agreement.

Ref. PBS-0417 Live · under NDA
23,268
Square feet (±)
3
ISO 7 suites
1,000
L/hr WFI capacity
2019
FDA-inspected
503B
Outsourcing pathway

The opportunity

Built, equipped, inspected — and idle.

PBS-0417 is a non-operating cGMP sterile compounding facility in Southern California, purpose-built between 2015 and 2018 and FDA-inspected in 2019. It ran roughly a year of sterile production before pausing, and is offered fully built-out and equipped — ready to restart or convert.

The value is in what is already standing: three ISO 7 cleanroom suites, a 1,000-litre-per-hour Water-for-Injection system, and a documented FDA inspection history. It is positioned for financial sponsors and for strategic buyers — hospitals expanding into 503B, or pharmacies adding sterile and 503A capacity.

The replacement-cost case

You can't reproduce this quickly — or cheaply.

$28M–$56M+
Estimated cost to replicate
3+ years
To build, equip & qualify

Offered turnkey — the buildout, equipment, and inspection history already exist. The premium a buyer avoids is measured in years, not just dollars.

What you're acquiring

The asset behind the thesis.

Physical and regulatory infrastructure that takes years to assemble — already in place.

Three ISO 7 suites

Cleanroom capacity purpose-built for sterile 503B production.

Water-for-Injection system

A 1,000 L/hr WFI system — among the hardest utilities to build and qualify.

cGMP construction

Purpose-built 2015–2018 to current good manufacturing practice standards.

FDA inspection history

Inspected in 2019 — a documented federal regulatory footprint.

503B outsourcing pathway

Positioned for outsourcing-facility sterile production at scale.

Turnkey & non-operating

Built and equipped, ready to restart or convert — no ground-up build.

At a glance

The blind-teaser snapshot.

SectorcGMP sterile compounding (503B)
RegionSouthern California
Size± 23,268 SF
Cleanrooms3 × ISO 7 suites
Water systemWFI · 1,000 L/hr
Construction2015–2018
FDA inspection2019
Regulatory pathway503B outsourcing
StatusNon-operating · turnkey
Prior operation~1 year sterile production
Replicate cost≈ $28M–$56M+
StructureSuccess-fee sell-side

Released under NDA

Entity name and address, equipment schedules, real-estate and lease terms, inspection documentation, and the full confidential information memorandum are shared only with qualified buyers under a mutual non-disclosure agreement.

Mandate PBS-0417

Request the confidential memorandum.

Qualified buyers receive the full CIM — facility detail, equipment, and the replacement-cost analysis — under a mutual NDA. Start with a confidential conversation.

Request the CIM under NDA