JAVNO NAROČANJE ZDRAVIL

Gorjup, Iris

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Title:	JAVNO NAROČANJE ZDRAVIL
Authors:	ID Gorjup, Iris (Author) ID Kranjc, Vesna (Mentor) More about this mentor...
Files:	MAG_Gorjup_Iris_2016.pdf (1,64 MB) MD5: 753998AFB2570220C5DB8D3BD4490AE4
Language:	Slovenian
Work type:	Master's thesis
Typology:	2.09 - Master's Thesis
Organization:	PF - Faculty of Law
Abstract:	Področje preskrbe z zdravili je zaradi svoje pomembnosti, to je varovanja javnega zdravja, urejeno s številnimi področnimi predpisi, ki jih je potrebno upoštevati tudi pri izvajanju postopka oddaje javnega naročila za dobavo zdravil. V magistrski nalogi so predstavljene posebnosti, ki jih je potrebno, glede na podrobno področno zakonodajo, vključiti v razpisno dokumentacijo, in sicer posebnosti pri oblikovanju predmeta javnega naročila, kjer je potrebno med drugim upoštevati tudi zakonsko delitev zdravil na registrirana in neregistrirana zdravila, posebnosti pri oblikovanju tehničnih specifikacij, poseben poudarek pa je podan tudi vprašanju oblikovanja merila za izbor najugodnejše ponudbe, ter usklajevanju pogodbenih cen, saj so cene zdravil zakonsko regulirane. Ker se v zadnjem času vse bolj odražajo težnje po skupnem javnem naročanju zdravil, ki je postalo obvezno tudi za javne zdravstvene zavode, je v magistrski nalogi predstavljena pravna problematika, ki se pojavlja pri skupnem javnem naročanju. Bistvena posebnost pri preskrbi z zdravili pa je tudi distribucija zdravil, ki poteka preko veledrogerij, ob čemer pa zakon natančno določa pogoje, ki morajo biti ob tem izpolnjeni. Predstavljeno je tudi posredništvo v prometu z zdravili, ki je na novo urejeno v Zakonu o zdravilih (Uradni list RS, št. 17/14) in vzporeden uvoz zdravil, ter pogoji, ki morajo biti pri tem izpolnjeni. Načelo o prostem pretoku blaga, ki je eno od temeljnih načel evropskega pravnega reda, v primeru zdravil namreč ne velja na enak način kot to velja za pretežno večino ostalih izdelkov.
Keywords:	javno naročanje, zdravila, Zakon o zdravilih.
Place of publishing:	Maribor
Publisher:	[I. Gorjup]
Year of publishing:	2016
PID:	20.500.12556/DKUM-59163
UDC:	347.451.8:616(043.2)
COBISS.SI-ID:	5188395
NUK URN:	URN:SI:UM:DK:CKYSGOQP
Publication date in DKUM:	15.09.2016
Views:	2372
Downloads:	407
Metadata:
Categories:	PF
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Secondary language

Language:	English
Title:	PUBLIC PROCUREMENT OF MEDICINE
Abstract:	The scope of supply of medicinal products, because of its importance to the protection of public health, is governed by numerous sectoral regulations, which must be taken into account in the implementation of the public procurement procedure for the supply of medicines. The thesis presents specific features which, according to the detailed sectoral legislation, must be included in the tender documentation, namely specificities in defining the object of the contract, where it is necessary to take into account the statutory division of registered and unregistered medicines, the peculiarities in the design of technical specifications, which is also governed by a number of sectoral regulations. Special emphasis is given also to the issue of award criteria and the prices of regulated drugs. Because og recent aspirations of the joint procurement of medicines, which became mandatory for public health institutions, the thesis also presents a legal problem which occurs in the joint procurement. An essential feature in the supply of medicines is also a question of distribution of medicines via wholesalers, while the law specifies the conditions that must be met. The thesis also presents brokering in trafficking of drugs, which is newly arranged in the Medicinal Products Act (Official Gazette of RS, no. 17/14) and parallel imports of medicines and the conditions that must be met. The principle of free movement of goods, which is one of the fundamental principles of the Community acquis, does not apply in the case of medicinal products in the same way as it applies to the majority of other products. The principle of free movement of goods, which is one of the fundamental principles of the Community acquis, does not apply in the case of medicinal products in the same way as it applies to the overwhelming majority of other products.
Keywords:	public procurement, medicines, Medicines act.

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