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Rita Lupu

Engineering and Quality Solutions. For the Medical Device Industry and. For the Pharmaceutical Industry. Establishing, Implementing and Maintaining Quality Systems and Products to be compliant with:. US / EU / CA / JP / IL Medical Device Regulations. US / EU Pharmaceutical Regulations. US / EU GLP Regulations. Quality Management System Standards. FDA / ICH / GAMP / PIC/S / GHTF guidelines. Preparing and Escorting External Audits. Device Design History Files. Drug Site Master Files.

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Rita Lupu | qualla.biz Reviews
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Engineering and Quality Solutions. For the Medical Device Industry and. For the Pharmaceutical Industry. Establishing, Implementing and Maintaining Quality Systems and Products to be compliant with:. US / EU / CA / JP / IL Medical Device Regulations. US / EU Pharmaceutical Regulations. US / EU GLP Regulations. Quality Management System Standards. FDA / ICH / GAMP / PIC/S / GHTF guidelines. Preparing and Escorting External Audits. Device Design History Files. Drug Site Master Files.
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2 risk management standards
3 software development standards
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6 developing
7 device registration files
8 device production files
9 drug production files
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Rita Lupu | qualla.biz Reviews

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Engineering and Quality Solutions. For the Medical Device Industry and. For the Pharmaceutical Industry. Establishing, Implementing and Maintaining Quality Systems and Products to be compliant with:. US / EU / CA / JP / IL Medical Device Regulations. US / EU Pharmaceutical Regulations. US / EU GLP Regulations. Quality Management System Standards. FDA / ICH / GAMP / PIC/S / GHTF guidelines. Preparing and Escorting External Audits. Device Design History Files. Drug Site Master Files.

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Engineering and Quality Solutions. For the Medical Device Industry and. For the Pharmaceutical Industry. Establishing, Implementing and Maintaining Quality Systems and Products to be compliant with:. US / EU / CA / JP / IL Medical Device Regulations. US / EU Pharmaceutical Regulations. US / EU GLP Regulations. Quality Management System Standards. FDA / ICH / GAMP / PIC/S / GHTF guidelines. Preparing and Escorting External Audits. Device Design History Files. Drug Site Master Files.

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