
Conducting your Clinical Trial at International Standards in Africa and Europe.
Expanding your Pharma Company Business in Africa.
Clinical Trials / Studies - Pharmaceuticals Marketing - Training
Access Programs - Bioequivalence Studies
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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