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Since its foundation, JC Automation has provided a full range of compliance and manufacturing services to the Pharmaceutical, Biological and Medical Devices industry. These services include validation, qualification and commissioning as well as on-site support to Manufacturing SCADA systems. Our expertise on Information Technologies and Regulatory Compliant Requirements has made JC Automation the perfect partner to implement and support Automation and Computerized Systems in the Pharmaceutical, Biological and Medical Devices industry. Our suite of Compliance and Manufacturing System Services includes:
- Infrastructure system Validations (Servers, Workstations, Networks "LAN, WAN & MAN" and Premises Wiring)
- Computer Room Validations
- Design And Develop High Availability solution for Manufacturing/ Laboratory systems
- 21 CFR PART 11 Assessments and Validation
- VP, URS, TS, IQ, OQ, PQ and SOP Document Development
- Laboratory Equipment Validation Services
- Specialize Technical Writers Services
- Compliance Studies and Audits (e.g. CAPA investigations)
- GxP Computerized Systems Validation
- SCADA application development and validation services (eg. Wonderware / PLC / PanelView)
- Building Management Systems Validation
- Compressed Air Systems Commissioning
- Access Control Systems Commissioning
- USP Water Systems Validation
- Power Monitoring Systems Commissioning
- Information Security and Availability Solutions - Development, Implementation and Validation
- Citrix MetaFrame Administration, Implementation and Validation Services
- Manufacturing Systems Engineering and Support
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