CQV | Multiple Facilities Projects
- Area: Greater Los Angeles
- Project Type: CQV
About this Project
OBJECTIVE
Commissioning, Qualification, Validation (CQV)
SERVICES
PSC® has been an essential service provider to client throughout the development and implementation of a new cell and gene therapy manufacturing facility. PSC® joined the project during the planning phase and conducted critical design review to ensure facility met cGMP expectations upon completion. Our consultants worked closely with architects, engineers, contractors, and equipment vendors to develop system turnover packages to support subsequent commissioning and qualification efforts. PSC® then performed commissioning and qualification of all facility, utility, and process systems to meet GMP production timelines.
EQUIPMENT USED
- Kaye Validator
- Additional SIM for Kaye 2000
- iRTD-400 Probe
- LTR-140 Bath
- HTR-400 Bath
- Data Loggers
- Kaye Feed Thru Device
- Pressure Transducer
- CLiMET (laser particle counter)
- Low Pressure Gas Flowmeter
- CLiMET (Microbial Sampler)
- Shortridge Air Data MultiMeter
- Druck Pressure Testing
- Gas Flowmeter
- SVMS Steam Quality
- Thermocouples
- Scissor Lift
- Specialized PPE
- Specialized Tools
PROJECT SUCCESS
PSC® successfully supported the client’s project to develop a brownfield property into a cell and gene therapy manufacturing facility, performing cGMP operations for clinical trial material production within an aggressive timeline. PSC® partnered with the client and multi-discipline team members throughout the project life-cycle to achieve this success.
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