Regulatory, Study documents Creation and Study Approval
ACTG-CRO ensures 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].
ACTG-CRO creates 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.