Every amenity at our Wilmington and Cork sites exists to support one outcome: a batch record that holds up to scrutiny, every time.
Positive-pressure cleanroom suites for aseptic filling and packaging operations.
In-house HPLC, mass spec, and dissolution testing for full batch release authority.
Monitored 2-8°C and -20°C storage with continuous data logging and alarm failover.
Dedicated quality assurance team signs off on every batch before it leaves the site.
SCADA-monitored production lines with full audit-trail logging on every parameter.
Badge-controlled, logged entry to every production and storage zone on site.
Dedicated training rooms for GMP certification and ongoing staff competency review.
Continuous particulate, temperature, and humidity tracking across all controlled spaces.
Our facilities were designed around the regulatory standard, not retrofitted to meet it. Materials flow in one direction, personnel and product never cross paths unnecessarily, and every room maps directly to a step in the batch record.
It's a quieter kind of amenity — but it's the one our auditors notice first.
Schedule a Facility TourWe've toured a dozen contract manufacturing sites. Seven Pharmacist's was the first where the facility layout itself made the quality story obvious before anyone said a word.Quality Director, Prospective Partner