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Clinical Manufacturing
High Quality, Efficient & Reliable Manufacturing
Our GMP manufacturing team is expert at producing high quality cell and gene therapy products for use in clinical trials. The team consists of qualified aseptic operators who have years of experience in biologic manufacturing and have been carefully trained and onboarded by the BioCentriq team.
Manufacturing is supported by an experienced and knowledgeable supply chain management team who have established vendor relationships and will efficiently and expertly source the materials required for your program. We also have investigators who will facilitate the assessment of any deviations that occur and a training team that ensures operators assigned to your program are trained in project specific unit operations and qualified to support your process.
Why Choose BioCentriq?
Our hybrid model allows you to observe or work alongside our operators.
BioCentriq's in-house training team develops skilled and qualified operators.
Our global vendor relationships are leveraged to address supply chain challenges.
What Phases of Clinical Manufacturing Does BioCentriq Support?
The BioCentriq manufacturing team, processes, equipment and facilities are currently designed to support all phases of pre-clinical and clinical manufacturing. We are currently readying our facilities and systems to support commercial manufacturing starting in 2024.
Key Features of Our Manufacturing Capability
The BioCentriq Team
The manufacturing team at BioCentriq includes highly experienced operators who are qualified in aseptic technique, GMP procedures and GDP. In addition, we are fortunate to have seasoned leaders and supervisors who bring significant value to all our clients.
BioCentriq's New Jersey location gives it superior access to a pool of trained personnel coming from nearby big pharmaceutical companies who are downsizing or transitioning their manufacturing.
Learn more about our people.
"My goal is to ensure your product's integrity from start to finish, keeping in mind the potential your product will have to change patients' lives."
Robert Braddock
Senior Director of Manufacturing Operations
“I combine my time spent at Bristol Meyers Squib and BioCentriq to offer the client's I work with valuable experience that will usher their product into clinic, treating each project as if it were my own."
Nagla Hermida
Production Supervisor
Newly Constructed, Modern Facilities
BioCentriq has two state-of-the-art, newly constructed facilities for cGMP manufacturing.
We have two clean room manufacturing suites and supporting infrastructure in Newark, NJ and two more suites, soon to be three, in South Brunswick, NJ which also houses our pilot plant, analytical method development and QC laboratory.
