Login
Register
Reset Password
Publish & Distribute
Publishing Solutions
Distribution Solutions
Subjects
Architecture and Design
Arts
Business and Economics
Chemistry
Classical and Ancient Near Eastern Studies
Computer Sciences
Cultural Studies
Engineering
General Interest
Geosciences
History
Industrial Chemistry
Jewish Studies
Law
Library and Information Science, Book Studies
Life Sciences
Linguistics and Semiotics
Literary Studies
Materials Sciences
Mathematics
Medicine
Music
Pharmacy
Philosophy
Physics
Social Sciences
Sports and Recreation
Theology and Religion
Publications
Journals
Books
Proceedings
Publishers
Blog
Contact
Search
EUR
USD
GBP
English
English
Deutsch
Polski
Español
Français
Italiano
Cart
Home
Journals
Archives of Industrial Hygiene and Toxicology
Volume 61 (2010): Issue 3 (September 2010)
Open Access
New European Commission Regulation on Variations to the Terms of Marketing Authorisation for Medicinal Products and its Impact on Croatian Legislation
Adrijana Martinac
Adrijana Martinac
,
Siniša Tomić
Siniša Tomić
and
Mirna Šimičić
Mirna Šimičić
| Sep 22, 2010
Archives of Industrial Hygiene and Toxicology
Volume 61 (2010): Issue 3 (September 2010)
About this article
Previous Article
Next Article
Abstract
References
Authors
Articles in this Issue
Preview
PDF
Cite
Share
Published Online:
Sep 22, 2010
Page range:
311 - 322
DOI:
https://doi.org/10.2478/10004-1254-61-2010-2015
Keywords
djelotvornost
,
dokumentacija o lijeku
,
kakvoća
,
sigurnost
,
Zakon o lijekovima
This content is open access.
Adrijana Martinac
Agency for Medicinal Products and Medical Devices, Zagreb
Siniša Tomić
Agency for Medicinal Products and Medical Devices, Zagreb
Mirna Šimičić
Jadran Galenski Laboratorij d.d., Rijeka, Croatia