About Us
Huntsville, AL Facility
Development and contract manufacturing, packaging, and warehousing of non-sterile liquids and semi-solids from TriRx’s best-in-class pharmaceutical facility in the southeastern United States.
Shawnee, KS Facility
Drug product manufacturing and packaging facility offering sterile and non-sterile liquids, parenteral, oral solid dose (OSD), and topicals manufacturing for the human and animal health markets.
Segré, France Facility
Sterile and non-sterile pharmaceutical manufacturing and integrated packaging of liquid and semi-solid drug products.
Speke, Liverpool Facility
Drug substance facility offering state-of-the-art biopharmaceutical production; services offered include fermentation, spray drying, coating, pre-mixing and large molecule biologics (mAbs, recombinant proteins). This facility is located in one of the UK’s leading bioprocessing regions.
TriRx Pharmaceutical Services is a contract development and manufacturing organization (CDMO) committed to creating a better outsourcing experience for customers in the human and animal health pharmaceutical industries.
More Than A Pharmaceutical Services Provider
TriRx was built on the principles of honesty, transparency, and integrity. Headquartered in Norwalk, Connecticut, and with an expanding network of development and manufacturing facilities worldwide, we believe customers who entrust their products to us deserve more than a contract service provider but a long-term partner for contract pharmaceutical services. That is why TriRx serves as both your manufacturing arm and your advocate, giving you the assurance that we will take care of your product as if it were our own.
DELIVERING ON OUR PROMISES
Our team is able to execute our philosophy because we have operated on both sides of a CDMO–innovator relationship. TriRx was founded by a team of pharmaceutical industry veterans with extensive experience as both contract service providers and CDMO customers. We understand what it’s like to entrust your product to a contract manufacturer, and we take that responsibility seriously. You can count on us to deliver—on time, in full, at the agreed-upon price and scope, and to the highest quality and regulatory standards.
Global Regulatory Approvals
- FDA
- DEA
- ANSES (France)
- EMA
- ISO 9001
- Russia
- MHLW (Japan)
- ANVISA (Brazil)
- Health Canada
- APRA (Australia)
- VMD (UK Veterinary Medicines Directorate)
- Ministry of Food, Agriculture and Livestock (Turkey)
- Medsafe (New Zealand)
- FAMI-QS and SF/SF (Feed safety management systems)
Advanced
Approach
Our Values
People are at the core of our business. We are able to serve our customers and, ultimately, patients because of our staff’s exceptional performance and dedicated contributions.
Excellence
We deliver quality products that meet or exceed regulatory requirements and have a passion for operational excellence and continuous improvement in all that we do.
Respect for People
We value our people, encourage their development, and reward their performance and contribution. We treat others the way we want to be treated.
Teamwork
We value our team’s collective wisdom and capabilities; we work together as scientists, engineers, project managers, and technologists to deliver on our promises.
Community
TriRx works hard to make our facilities into innovation hubs for our staff and the greater communities in which we work and live.
Integrity
We know and do what is right. TriRx prides itself on going above and beyond for each project instead of cutting corners.
Customer Service
Being a pharma CDMO you can trust means constant, proactive communication. We work as an extension of your team to deliver on-time results.
Advance the Conversation
Get in touch with our team and discover how we can support your long-term success. Whether you need help with a specific project, want to learn more about our facilities, or just want to set up a meeting, send us a message below to get started.