ID Pharma represents the Marketing Authorization Holder in Poland, providing support for pharmacovigilance processes and medical information dedicated to the Polish market,

Ensuring compliance with Polish requirements, European regulations and procedures of the Marketing Authorization Holder.

• acts as a local contact point for regulatory authorities ensuring the availability 24/7;

• answers medical inquiries;

• processes reports on adverse drug reactions in Poland.

We cooperate with consultants / companies based in other EU and non-EU markets, providing 24/7 access to a person who provides medical information in the national language and is included in the adverse drug reaction management system.