Agencija za lekove i medicinska sredstva Srbije (ALIMS) je 02.04.2026. godine objavila obaveštenje o unapređenju postupka izdavanja stručnih mišljenja iz oblasti medicinskih sredstava.
U cilju efikasnijeg i standardizovanog procesa, izmenjen je način podnošenja zahteva. Od sada je obavezno unošenje podataka o proizvodu i proizvođaču/ino-isporučiocu kroz aplikaciju ADIS.
Detaljnija uputstva o načinu podnošenja zahteva dostupna su u sekciji REGULATIVA / MEDICINSKA SREDSTVA / Uputstva (redni broj 7) na zvaničnom sajtu ALIMS-a.
ENGLISH VERSION
Changes in the procedure for submitting requests for expert opinions on medical devices. The Medicines and Medical Devices Agency of Serbia (ALIMS) announced on April 2, 2026, an update to the process for issuing expert opinions in the field of medical devices.
In order to ensure a more efficient and standardized procedure, the method of submitting requests has been modified. From now on, it is mandatory to enter product and manufacturer/foreign supplier data through the ADIS application.
Detailed instructions on how to submit requests are available in the section REGULATIONS / MEDICAL DEVICES / Guidelines (item no. 7) on the official ALIMS website.
