欧洲药品管理局公布了其计划给予公众获取信息的数据库的潜在副作用的人力和兽医药品。
The European Medicines Agency has published its plans for granting public access to the information held in its databases of the potential side effects of human and veterinary medicines.
对人类和兽医药品，该机构将考虑提供访问数据用于研究目的的个案的基础上，根据其目的是保护公众健康。
For both human and veterinary medicines, the Agency will consider providing access to data for research purposes on a case-by-case basis, in line with its objective of protecting public health.
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