CRO Services - ACTG-CRO

Regulatory, Study documents Creation and Study Approval

We ensure the submission and follow-up of the files under the best conditions to the competent committees and regulatory authorities [DPM (in Tunisia DPM corresponds to the ANSM in France), CPP, Ethic Committees, etc]. We create study documents according to the rules in force: observation books, information note, consent collection form, etc. Where appropriate, we propose the establishment and management of e-CRFs. 

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Clinical Research, Tunisia, Africa, Clinical Trials, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical

Conducting your Clinical Trial at International Standards in Africa.

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