REGULATORY AFFAIRS


We are a leading company in regulatory affairs services for Serbia.

We are the only local company whose experts were engaged in founding Medicines Agencies
on the territory of ex Yugoslavia and establishing EU regulative in the Republic of Serbia and neighbor countries.

We will advice you on all aspects in the preparation of registration dossiers for medicines and medical devices, ranging from feasibility studies, clinical trials and registration, right up to
post-marketing surveillance.

We can handle any registration or regulatory project in our region.

Let us and our team of associated experts guide you through the regulatory system.

For our references in the regulatory affairs, see Regulatory - references.



For further information, assistance or explanation, please contact: pedja@polifarm.rs






Regulatory Affairs Services Registration of medical devices Drug registration. Serbia Drug Registration OTC registration. Serbia Srbija Medical devices registration. Serbia Srbija Regulatory Affairs Serbia Drug Registration The Agency Medical Devices Registration Regulatory References Drugs Medical Devices Serbia Srbija Pharmacy Consulting Pharmacy Serbia Regulatorni poslovi Srbija Agencija za Lekove i medicinska sredstva Registracija lekova u Srbiji Regulativa reference Lekovi registracija Medicinska sredstva registracija konsalting farmacija Srbija Agencija lekovi registracija Registration of OTC products
 
 
 
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