Review draft · not published · copy pending client approval

About the laboratory

A working site with a long record.

TPP Tech operates a sterile injectable manufacturing site in San Diego with an on-site analytical laboratory. We manufacture under contract and we test — identity, purity, content and safety — for compounding pharmacies, product developers and research-use suppliers.

The company

Three decades of manufacturing in San Diego.

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.

1990sContinuous cGMP operation begins in San Diego
2015Operations move to the current Nancy Ridge Drive facility
2023FDA inspection passed
TodayTPP runs manufacturing and analytical testing from the facility

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

Manufacturing and CDMO services are on the TPP CDMO manufacturing site

HPLC stack with a sample vial
HPLC
Facility exterior, Nancy Ridge Drive
Nancy Ridge Drive
Vial filling line
Vial filling line

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.

Jan 2023

FDA inspection

Most recent inspection passed.

DEA

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.

In-house

cGMP QC & analytical labs

Chromatography, spectroscopy, dissolution, particle-size, TOC, DSC/TGA — method development through release testing.

Visit the site

Come see the facility.

We host sponsor visits and quality audits by appointment.

Email
info@tppcdmo.com
Phone
858-623-1520
Address
6828 Nancy Ridge Drive #100
San Diego, CA 92121