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Medical Device Clinical CRO

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Clinical Trial Preparation

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Clinical trial protocol writing

Hospital site screening

Researchers' meeting

Ethics committee meeting

Genetic office record

Provincial bureau record

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Clinical Trial Implementation

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Clinical trial conducted

Experimental product management

Clinical trial start-up and monitoring

Subject recruitment

Clinical trial quality control

EDC data entry

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Summary of Clinical Result

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Medicine inspect

Data audit

Database lock

SAS programming

Data management

Data statistics

Clinical trial report

Final report entitled

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