Support Services for FDA/EU Inspections and a Professional Service Agreement with Jacobs
Chiyoda’s technologies, developments, achievements and approach to new projects
Chiyoda supports pharmaceutical manufacturers who have obtained FDA/EMA inspection and European CE marking certification, as detailed below:
- Mock Audit/Consultation Operation Services
- Support for FDA Pre-meetings/Witnessing
- Good manufacturing practice (GMP) Consulting Services
- Validation Support
- FDA/EU Inspection Support
- Professional Service Agreement with Jacobs
Chiyoda adheres to the ever-changing good manufacturing practice (GMP) requirements for pharmaceutical manufacturing, and incorporates them into facility designs and validation, through its partnership with Jacobs, one of the world’s largest and most diverse providers of technical, professional and construction services for pharmaceutical production facilities.
Our Business
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- Metals and Materials
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- Life Science
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- Pharmaceutical
- Biopharmaceuticals
- Middle Molecule Drugs
- Regenerative Medicine
- Synthetic API
- Sterile Pharmaceuticals
- Solid / Topical Pharmaceuticals
- Cutting-edge Isolation Technology
- Simulations
- GMP / Validation
- Packaging
- Logistics and Material Handling
- Manufacturing Execution Systems (MES) Package ’PAS-X’
- Support Services for FDA/EU Inspections and a Professional Service Agreement with Jacobs
- Technical Consulting
- O&M-X Solutions
- Technologies and Solutions