PROJECT START-UP - ACTIVA-CRO

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Advice on Study Design, Protocol ,ICF & CRF/eCRF development
Clinical Development Plans (PM, Monitoring, Quality, Communication, etc)
Final Investigator/site selection & patient recruitment strategies

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Preparation and conduction of Kick off meeting.
Investigator Meeting Planning and execution
Timely submission of regulatory Dossiers to IRB’s/ECs/MOH to ensure the lowest timeframe from study set-up to FPI

Activa CRO

Offers full service in the field of Clinical research, bringing outsourcing solutions to the Pharmaceutical, Drug, Biological and Device Industry.