欧盟免疫兽药产品的许可程序。

Advances in veterinary medicine Pub Date : 1999-01-01 DOI:10.1016/s0065-3519(99)80045-7

P P Pastoret, F Falize

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引用次数: 4

摘要

随着新的授权制度的采用，所有兽药产品的监管需求都得到了欧盟的满足。这一制度确实为创新产品，特别是疫苗，提供了进入全大陆市场的机会，并为其他产品进入会员国市场提供了便利。这将对兽医疫苗行业产生明显的有利影响。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Licensing procedures for immunological veterinary medicinal products in the European Union.

With the adoption of the new authorization system, all regulatory needs for veterinary medicinal products have been fulfilled with the European Union. This system, indeed, provides access to a continent-wide market to innovative products, in particular vaccines, and facilitates access to the markets of the Member States for other products. This should have a clearly favorable impact on the veterinary vaccines industry.

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Advances in veterinary medicine

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