Location: North America/Europe/Asia
Area: N/A
Project Cost: Confidential
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This client boasts state-of-the-art facilities to manufacture various injectable vaccine products.
PharmEng provided the cGMP, engineering, validation, and design expertise to ensure that the client’s facilities met regulatory requirements.
- Provided validation services & cGMP expertise on a new vaccine production facility
- Provided expertise on vaccine production equipment validation
(Includes bioreactors, fermentors, clean-in-place skids, column chromatography skids, and others)
- Completed a Cleaning Validation Project for a bin blending suite equipment
Responsibilities:
- Computer Validation (New & Legacy Equipment)
- Equipment Validation
- Building Utility Systems Validation
- Warehouse Temperature Mapping
- Laboratory Instrument Validation
- Cleaning Validation
- FDA PAI Audit
Location:
North America/Europe/Asia
Area:
N/A
Project Cost:
Confidential
Bio-containment level:
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