Clintriox Research Solutions Inc.
solutions, Clinical Trials, clinical research
Pre Study: Site recruitment Site Initiations Ethics submission process CTA review Budget preparation Contract negotiations Liasion with Sponsor Clinical Study coordinating: Patient screening/identification Consent process Source documents CRF filling and submission AEs and SAEs reporting Attendance at the monitoring visit Liaison with the research ethics board Post Study: Study close out Audits Post trial follow up Query resolution Documents storage
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