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g-docs™ GCP
Good clinical practice is a set of internationally recognised ethical and scientific quality requirements which must be observed for designing, conducting, recording and reporting clinical trials that involve the participation of human subjects.
Click here> to see the GCP process video
In order to ensure the credibility of the data generated in the trial and to provide control of documents for successful eTMF and eCTD submission g-docs GCP can be used by Sponsor companies and CRO’s alike