TRI · Korea

Supporting Korean Biomanufacturing

Leading the way

ENTRI is transforming the biomanufacturing landscape

The purpose-built cGMP commercial and clinical manufacturing facility supports emerging and maturing biotech and medtech companies.

ENTRI gives companies the ability to accelerate their success. Providing access to world-class infrastructure, facilities designed to meet global cGMP standards, and technical wrap-around support, companies can scale their manufacturing with confidence.

Enquiries for tenancy are welcome. Available for occupation from Q2, 2026.

Email Dr Ryan Parlett, Head of Commercial Operations, below to express your interest, or complete the form at the bottom of this page.

Email Dr Ryan Parlett to express your interest in ENTRI.

Clinical & commercial manufacturing

ENTRI supports analytical and process development, drug substance (DS), drug product (DP), manufacturing, and on-site Quality Control, including:

Biologics: ADCs, bioconjugates and mAbs.

Cell and gene therapies: CAR T-cell therapies, iPSC-based products, extracellular vesicles (EVs).

RNA-based products: mRNA-LNPs.

Drug-device combination products. Other product types may also be supported, subject to facility fit.

World-class infrastructure

ENTRI offers cGMP cleanrooms, wet labs (PC2 compliant), and office spaces.

Spread over four levels and more than 7,000 m2 (75,000 ft2), ENTRI adheres to TGA and PIC/S-aligned manufacturing standards within quality-controlled environments.

ENTRI offers scalable manufacturing infrastructure and supports multiple modalities, which adapt to suit tenants’ needs.

Infrastructure and facilities, including cGMP cleanrooms, wet labs, and office spaces, are licencible for tenants’ exclusive use.

Navigate ENTRI

Innovation and Collaboration space

Flexible space able to support engineering and chemistry development; showcase/training for suppliers/vendors; events; warehousing and cGMP storage area
Level 1
 
Level 2
 
Level 3
 
Level 4

Infrastructure & capabilities

Non-CDMO Model

Enhanced Control: Maintain full oversight of critical production processes and manufacturing intellectual property.

Compliance: Facilities meet cGMP and global regulatory standards.

Flexibility: Easily adapt to changing production demands, schedules, and timelines.

Dedicated Capacity: Secure guaranteed manufacturing capacity to use across pipeline assets.

Clinical Trials Network

ENTRI can accelerate speed to clinic.

Access state-of-the-art adult and paediatric clinical trial units through TRI’s partners, and within the expansive Queensland’s clinical trial network.

Read more about:

Clinical Research Facility

Paediatric Clinical Trials

Operations

Retain IP & Control

ENTRI offers a disciplined alternative to a CDMO model. Companies that choose to base their operations at ENTRI retain the intellectual property rights to their manufacturing processes and products.

Tenants are responsible for all regulatory approvals, including those from the TGA.

Australia offers pharmaceutical patients for up to 25 years, which protects the IP rights of both the creators and owners.

Partners

TRI

Life Science Ecosystem

Australian Ecosystem

Government Support

Submit an expression of interest.