REGULATORY READINESS
Registered. Licensed.
Quality focused.
Pharmaceutical packaging demands a strong compliance foundation. UDS maintains regulatory registrations and licenses supporting its packaging services, including controlled-substance programs.
FDA
FDA-Registered Facility
Pharmaceutical repackaging operations conducted under applicable FDA and current good manufacturing practice (cGMP) requirements.
NC
North Carolina Licensing
North Carolina state pharmaceutical and controlled-substance licensing applicable to UDS operations.
DEA
DEA Schedules II–V
DEA registration supporting authorized handling and packaging of Schedule II through V controlled substances, subject to applicable requirements.
US
Multi-State Licensing
Additional out-of-state licenses and permits supporting customer programs in multiple jurisdictions.
Specific registrations, licenses, permitted activities, and state coverage are confirmed by UDS for each project. FDA registration does not constitute FDA approval of a facility or its products.