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The manufacturing suites are comprised of complete, large scale
process manufacturing equipment to produce granulations, beads,
spheres, or tablets. The facilities are cGMP with registration
and inspection by the FDA.
The manufacturing suites have been constructed to meet ISPE
Baseline Pharmaceutical Guidelines. Provisions have been made
with the DEA for handling Schedule II-V - Controlled Substances.
Products developed and scaled up in the R&D/Pilot Suites
may be transferred to the manufacturing suites as a SUPAC Level
1 transfer. No site change approvals are required.
Click
here for a detailed equipment list
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