Granting marketing authorisation for medicines in South East European countries: The point of view of the authority-Reference-Cited by-同舟云学术

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Granting marketing authorisation for medicines in South East European countries: The point of view of the authority

Published:2010-07 Issue:2-3 Volume:57 Page:325-332
ISSN:0273-2300
Container-title:Regulatory Toxicology and Pharmacology
language:en
Short-container-title:Regulatory Toxicology and Pharmacology

Author:

Tomić Siniša,Sučić Anita Filipović,Martinac Adrijana Ilić

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference26 articles.

1. Act on medicinal products and medical devices of Bosnia and Herzegovina, 2008. Official Gazette, 58/08.

2. Act on medicinal products and medical devices, 1997. Official Gazette of the Republic of Croatia, 124/97.

3. Act on medicinal products and medical devices, 2003. Official Gazette of the Republic of Croatia, 121/03.

4. Act on medicinal products, 2007. Official Gazette of the Republic of Croatia, 71/07.

5. Act on medicinal products and medical devices, 2007. Official Gazette of the Republic of Macedonia, 106/07.

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1. Impact of the European Union on access to medicines in low- and middle-income countries: A scoping review;The Lancet Regional Health - Europe;2021-10

2. Potential negative impact of reputed regulators’ decisions on the approval status of new cancer drugs in Latin American countries: A descriptive analysis;PLOS ONE;2021-07-13

3. Mutual recognition in the European system: A blueprint for increasing access to medicines?;Regulatory Toxicology and Pharmacology;2019-08

4. Medicine Availability and Prescribing Policy for Non-Communicable Diseases in the Western Balkan Countries;Frontiers in Public Health;2017-11-08

5. How to remove barriers to medicines trade in emerging economies: the role of medicines regulatory authority in Serbia;Accreditation and Quality Assurance;2011-01-15

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