About us


With our local presence in African countries, clients are guaranteed that their trials will be conducted according to international standards. We assign locally-based CRAs trained to clinical trials regulations and SOPs (both company and sponsor SOPs).

The fact we run operations from Tunisia, apart from Europe, US enables us to provide very competitive rates.

We provide you Clinical Sites to implement your trial.

With our Expertise in clinical trials and our list of Experienced Investigators specialized in a range of therapeutic areas with whom we entertain great relationships, we are ensuring to provide the services you need with the excellent process.

We have great relations with Regulatory Authorities, Ethics Committees and we know the local process for documents submission.

We are in close contact and cooperating with the Ministry of Health of Tunisia.

We have comprehensive and detailed SOPs to guide and train all the staff, to ensure operations to be carried out in compliance with ICH/GCP Regulations and to fulfill Sponsor requests and requirements.

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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