TPP CDMO
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ABOUT TPP

Three decades of manufacturing in San Diego.

TPP's San Diego operation has made medicines in the United States continuously for over 30 years. Our work now is bringing more of the world's drug development and supply onshore.

1990s
Continuous cGMP operation begins in San Diego
2015
Operations move to the current Nancy Ridge Drive facility
2023
FDA inspection passed
TODAY
TPP runs manufacturing and analytical testing from the facility
THE COMPANY

A working site with a long record.

The operation has run under continuous cGMP since the 1990s, most recently as Societal CDMO San Diego, and has been at its current Nancy Ridge Drive facility since 2015. TPP acquired the site and now runs contract development and manufacturing and in-house cGMP (GLP) analytical testing from it.

The equipment, quality systems, and inspection history stayed. What changed is the mandate: TPP is focused on re-shoring pharmaceutical manufacturing and supply chains to the United States, and on giving global innovators a direct route into the U.S. market.

OUR PURPOSE

Advancing access to high-quality, cost-effective medicines for better U.S. healthcare outcomes.

TPP facility entrance, Nancy Ridge Drive
30+
years of U.S. manufacturing
24,400
sq ft of cGMP space
3
service lines
THE FACILITY

Development, manufacturing, and labs under one roof.

Sterile suite: formulation mixing, automated vial filling, lyophilization Oral solids: milling, blending, compression, encapsulation, coating Liquids: 2,000 L jacketed tanks, batches to 4,000 L cGMP QC and analytical laboratories Serialized packaging, controlled-temperature warehouse, DEA vaults
6828 NANCY RIDGE DRIVE, #100 · SAN DIEGO, CA 92121
Equipment and suites in detail →
Aerial view of the Nancy Ridge Drive business park, San Diego
TPP facility grounds, Nancy Ridge Drive
QUALITY & COMPLIANCE

The record, in the open.

Quality systems aligned with FDA, DEA, and international health authority requirements. Sponsors are welcome to audit; bring your quality team.

Request an audit date →
Jan 2023 FDA inspection
Most recent inspection passed.
DEA registered
Manufacturer: Schedule IV and V. Analytical lab: Schedule IV and V. On-site vaults.
≤ 3A SafeBridge potency
Containment and handling for potent compounds up to Category 3A across the cGMP footprint.
cGMP QC & analytical labs
Chromatography, spectroscopy, dissolution, particle-size, TOC, DSC/TGA — method development through release testing.
WHAT WE RUN

Manufacturing and analytical testing.

TPP CDMO Contract development & manufacturing → Formulation through commercial supply, multiple dosage forms. ANALYTICAL TESTING In-house cGMP (GLP) testing → Release, stability, and method development for sterile and oral products.
VISIT THE SITE

Come see the facility.

We host sponsor visits and quality audits by appointment. Or start with a program inquiry and we will respond within one business day.

Contact us Meet the leadership
INFO@TPPCDMO.COM 858-623-1520 6828 NANCY RIDGE DRIVE, SAN DIEGO
TPP CDMO

US-based pharmaceutical development and manufacturing in San Diego, California.

6828 NANCY RIDGE DRIVE, #100
SAN DIEGO, CA 92121
SERVICES
CDMO Services Analytical Testing
COMPANY
About & facility Leadership team Contact us
CONTACT
info@tppcdmo.com 858-623-1520 Client sponsored audits welcomed by appointment.
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