Controlled Substances
JHP is registered to process CIII, CIV and List I substances with well-established security and monitoring systems in place.
JHP Pharmaceuticals is proud of a 25 year heritage providing sterile contract manufacturing services including controlled substance manufacturing for the biotech and pharmaceutical industry.
Sterile Product Manufacturing Services:
- Aseptic Fill/Finish
- Lyophilization/Freeze-Drying
- Terminal Sterilization
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JHP is registered to process CIII, CIV and List I substances with well-established security and monitoring systems in place. The site has also completed numerous DEA audits and has robust expertise in controlled substance manufacturing, packaging and storage. Located in Rochester Michigan, JHP’s sterile manufacturing facility sits on over 80 acres and includes a 171,000 sq. ft. production building and 44,000 sq. ft. warehouse. JHP’s site has separate facilities for chemistry, sterility testing and microbiological testing providing customers with a variety of support services. |
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JHP Pharmaceuticals offers customers the Right Scale and Right Experience to meet controlled substance filling requirements. In choosing JHP, customers also have access to a comprehensive suite of support services including: Regulatory, Analytical Methods Development, Package Engineering, Stability Testing and Validation. |
Click Here To Download: • Fact Sheet: Controlled Substances |
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