Regulatory Affairs

Started in 1988 with a company of a different name by some members of the current team, who had already gained specific experience in industry realities in the field, this was our first area of consulting.

Medical writing

Through synergies with a team of experts (pharmacologists, clinicians, and pharmacists) we can support our Clients in the following activities


As required by European and Italian regulations, every AIC holder must have, on a stable and continuous basis, a pharmacovigilance service manager and is required to keep detailed records of all suspected adverse drug reactions observed in Italy, the European Union or a third country.

Affari Regolatori

MA registration

It began in 1988 with a company of a different name, but same Associates, our experience as an AIC-holding company. Records later sold to third parties for marketing include the following