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Global pharmaceutical and medical devices validation contracting business. Senior level Technical Writers with extensive experience writing validation documentation - URS, FRS, IQ, OQ, PQ, PV, CSV, SOPs, WI, MP, etc. We implement process from start to finish product - design, automation, parameters, to provide a repeatable & reproducible process. Calibration and PM expertise. DHJ Validation uses DHF, data analyses, statistical analysis of parameter settings, process engineering studies, etc.

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Global pharmaceutical and medical devices validation contracting business. Senior level Technical Writers with extensive experience writing validation documentation - URS, FRS, IQ, OQ, PQ, PV, CSV, SOPs, WI, MP, etc. We implement process from start to finish product - design, automation, parameters, to provide a repeatable & reproducible process. Calibration and PM expertise. DHJ Validation uses DHF, data analyses, statistical analysis of parameter settings, process engineering studies, etc.

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8 equipment qualifications

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Global pharmaceutical and medical devices validation contracting business. Senior level Technical Writers with extensive experience writing validation documentation - URS, FRS, IQ, OQ, PQ, PV, CSV, SOPs, WI, MP, etc. We implement process from start to finish product - design, automation, parameters, to provide a repeatable & reproducible process. Calibration and PM expertise. DHJ Validation uses DHF, data analyses, statistical analysis of parameter settings, process engineering studies, etc.

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Global pharmaceutical and medical devices validation contracting business. 21 CFR Parts Nov. 2Oct. 2Nov. 31Apr. 820. ISO 9000/116Jul. 13485May. 623Apr. 1497. GAMP-5, Annex 11, ASTM. FDA, EMEA, ICH, USP/NF, EP. VMP for Finished Products. System Develop Life Cycle. Automated Packaging and Labeling Systems. Automated Filling, Vial, Capping, and Bottling Systems. Process and Equipment Parameter / Specifications. Packaging Insert Labels (PILs). Validation Documentation - Writing and Execution.

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Global pharmaceutical and medical devices validation contracting business. Senior level Technical Writers with extensive experience writing validation documentation - URS, FRS, IQ, OQ, PQ, PV, CSV, SOPs, WI, MP, etc. We implement process from start to finish product - design, automation, parameters, to provide a repeatable & reproducible process. Calibration and PM expertise. DHJ Validation uses DHF, data analyses, statistical analysis of parameter settings, process engineering studies, etc.

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Global pharmaceutical and medical devices validation contracting business. Senior level Technical Writers with extensive experience writing validation documentation - URS, FRS, IQ, OQ, PQ, PV, CSV, SOPs, WI, MP, etc. We implement process from start to finish product - design, automation, parameters, to provide a repeatable & reproducible process. Calibration and PM expertise. DHJ Validation uses DHF, data analyses, statistical analysis of parameter settings, process engineering studies, etc.

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