Our Services

Medical and Regulatory Affairs

We are able to register your drugs and medical devices, as well as assist you in complying with regulatory requirements for public health markets in connection with health authorities in countries, WHO, and major donors (WHO Pre-qualification of Medicines, manufacturers qualification for public tenders, etc.).

We provide advice on the clinical standards required by health authorities and support you in setting up Phase IV clinical trials. 

We ensure the medical validation of your promotional campaigns, product training for field teams, including pharmacovigilance.

We can also offer medical support to marketing teams for review of medical reports and clinical studies, scientific communications, international congresses, as well as management of scientific experts/KOL.