查询词典 authorisations

Authorisations for access might be written into statute.

授权的访问可能会被写入章程。

The Seller and the Buyer shall take all steps reasonably necessary to obtain any authorisations required to be listed as a project participant as required under the International Rules.

买卖双方将采取所有合理的必要步骤以获得国际规则中规定的作为项目参与者所必备的授权。

Manufacturing Authorisations are required by all pharmaceutical manufacturers in the European Community whether the products are sold within or outside of the Community.

所有在欧盟内生产商必需获得市场授权，不论其产品是否在欧盟内销售。

Note: This Chapter deals with the responsibilities of manufacturers towards the Competent Authorities of the Member States with respect to the granting of marketing and manufacturing authorisations.

注： 本章主要介绍生产厂家对成员国负责发放销售许可证和生产许可证的主管部门的责任。

Supplier will provide all necessary authorisations, give assistance in the event of complaint, and reimburse ***** on request for all costs and expenses which may have been incurred to *****, including attorneys' and legal fees.

供应者将会提供所有的必需授权，提供在诉苦情况下的协助，和付还*****。

CHAPTER 5 PRODUCTION Principle 原则 Production operations must follow clearly defined procedures; they must comply with the principles of Good Manufacturing Practice in order to obtain products of the requisite quality and be in accordance with the relevant manufacturing and marketing authorisations.

生产操作必须按规定的程序进行，必须符合 GMP 的原则，以确保产品达到所要求的质量，并满足相关生产许可证和销售许可证的要求。

Analytical monitoring of process validations, process changes and new supplier authorisations.

对流程确认，工序变化及供应上授权进行分析和监管

When deciding upon an application for registration of a traditional herbal medicinal product, the Member State concerned should be obliged to take due account of authorisations or registrations previously granted by another Member State for that product.

在决定一个传统草药品的注册申请时，有关的成员国有责任适当考虑以前另一个成员国对该产品的授权和注册。

The overall content of the EDMF should contain detailed scientific information as indicated under the various headings of the relevnat Notice to Applicatns for Marketing Authorisations for Medicinal Products in the Member States of the European Union.

EDMF的的内容应当要包括详细的科学资料，这在相关的欧盟成员国的制剂上市许可申请者需知中的相关章节中有叙述。

I / We have the full authority from the Insured to provide the information requested on this application and to make the declarations, agreements and authorisations herein on behalf of the Insureds

本人 /我们获受保人授予全权，就本申请所需要提供资料，及在此以受保人名义，为本申请作出声明，签订同意及授权书，并就一切赔偿或一切按本申请所签发之保单的相

The basic concept of FOP can be summarized as to further optimize effective prescription according to the standard of curative effects and with the aid of modern science and technology and theories of traditional Chinese medicine.

其基本内涵可概括为：以确有疗效的中药复方为研究对象，以现代科学技术和传统中医药理论为技术支持，以该复方所治病证的药效响应为评价标准，以优化重组疗效更优的新复方为研究目的。

Ever since our world has been a world, native forests have been indiscriminately exploited by man.

自从我们的世界一直是世界原生森林被任意剥削人。