Alims ALiMS Vlada Republike Srbije
ALiMS
Documentation
Medical devices:

 Application Forms-Required medical devices MA documentation    Application Forms-Required medical devices MA documentation
 
 
 (In Serbian)
 Instructions for the preparation of documentation regarding the marketing authorization for a medical device with the CE marking.  Instructions for the preparation of documentation regarding the marketing authorization for a medical device with the CE marking.  Instructions for the preparation of documentation regarding the marketing authorization for a medical device with the CE marking.
 Instructions for the preparation of documentation regarding the marketing authorization for a medical device based on the regulations in force prior to the new Law on Medicinal Products and Medical Devices coming into force, those medical devices bearing the CE marking (in accordance with Article 159 of the existing Law).  Instructions for the preparation of documentation regarding the marketing authorization for a medical device based on the regulations in force prior to the new Law on Medicinal Products and Medical Devices coming into force, those medical devices bearing the CE marking (in accordance with Article 159 of the existing Law)  Instructions for the preparation of documentation regarding the marketing authorization for a medical device based on the regulations in force prior to the new Law on Medicinal Products and Medical Devices coming into force, those medical devices bearing the CE marking (in accordance with Article 159 of the existing Law)
 Instructions for the preparation of documentation for the marketing authorization for a medical device which is not compliant with regulations of the EU directives for medical devices, i.e. which do not have the CE marking.  Instructions for the preparation of documentation for the marketing authorization for a medical device which is not compliant with regulations of the EU directives for medical devices, i.e. which do not have the CE marking.  Instructions for the preparation of documentation for the marketing authorization for a medical device which is not compliant with regulations of the EU directives for medical devices, i.e. which do not have the CE marking.