EU 殺生物性製品規則の概要 - jetro.go.jp

eu殺生物性製品規則の概要 2015年4月 日本貿易振興機構（ジェトロ） ブリュッセル事務所 海外調査部 欧州ロシアcis課

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CEPAに関する制度情報 - jetro.go.jp

CEPAに関する制度情報 2012 年3月 日本貿易振興機構（ジェトロ） 香港事務所

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ジェトロハノイ メールマガジン - jetro.go.jp

1 ジェトロハノイ メールマガジン 2017 年3 月号 Vol.84 発行：日本貿易振興機構（ジェトロ）ハノイ務所 ベトナム農業ビジネスミッション

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英国法を準拠法とする契約書の作成と締結の注意点 ―日本と …

Copyright © 2015 JETRO. All rights reserved.

Unofficial translation - jetro.go.jp

© 2008, Pakorn Nilprapunt, Office of the Council of State (www.krisdika.go.th, www.lawreform.go.th) Remark: Reference to Thai legislation in any jurisdiction shall ...

(Garuda Emblem) Notification of Ministry of Industry ...

Unofficial Translation Only the Thai version of the texts is legally binding. Page 1 (Garuda Emblem) Notification of Ministry of Industry Subject: Hazard Classification and Communication System of Hazardous Substances B.E.

Specifications, Standards and Testing Methods for ...

Improvement of Agricultural Chemicals and Feeds (Law No. 35, 1953), which is stipulated under Paragraph 1 of Article 1-2 of the Agricultural Chemicals Regulation Law (Law No. 82, 1948), with such aims as adding to, mixing with, or infiltrating into feeds (the feeds stipulated

  Standards, Specification, Testing, Methods, Agricultural, Standards and testing methods

Specifications and Standards for Foods, Food Additives ...

Standards for Food and Food Additives etc.” is an important piece of legislation. Therein are set out all the specifications and standards for the following: foods; food additives; apparatus and containers/ packages; toys; and cleaning agents (detergents). As to the labeling of foods or additives, Article 21 (Standards for Labeling) of the

  Standards, Specification, Food, Specifications and standards for foods, Food additives, Additives, Standards and specifications

2018 年 主要国の自動車生産・販売動向 - JETRO

2018 年 主要国の自動車生産・販売動向 2019 年11 月 日本貿易振興機構（ジェトロ） 海外調査部 海外調査企画課

シンガポールにおける国際紛争を念頭においた 紛争解決条項 …

1 正式称は、「外国仲裁判断の承認および執行に関する条約」といい、以下の uncitral のウ ェブサイトによれば、平成26 年6 月の加盟国数は156 カ国。加盟国数の多さに加えて、アジア諸国

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Guidance on Preparation of a Product Registration …

An executive summary shall be provided with the common submission dossier template, which shall include the following information:- an overview, e.g., introductory descriptive information on the medical device, the intended uses and indications for use of the medical device,

  Dossiers, Template, Common, Submissions, Common submission dossier template

Home - Food and Drug Administration

(Common Submission Dossier Template) based on the provisions of AMDD. With the implementation of AO 2018-0002, the FDA through the Center for Device Regulation, Radiation Health and Research (CDRRHR) is also mandated to release list of medical devices per classification based on the classification set forth in the ASEAN AMDD.

  Dossiers, Template, Common, Submissions, Common submission dossier template

Guidance on the format of the risk management plan (RMP) …

the eCTD dossier of the supporting documents or PSURs , when applicable. Throughout the RMP template, eCTD data/submissions should be read as eCTD or CTD data/submission, corresponding to the type of submission to the competent authority. Specific requirements for different types of initial ... Where the submission of a common, consolidated RMP ...

  Management, Dossiers, Risks, Plan, Template, Common, Submissions, Risk management plan

Validation issues frequently seen with initial MAAs

If not, the applicant may use one of the proposed (invented) names or the common name (or scientific name), together with a trademark or the name of the Marketing Authorisation Holder. In both cases, the NRG review is required. Once the NRG review outcome is available, the dossier may be updated as required.

  Dossiers, Common

ASEAN MEDICAL DEVICE DIRECTIVE

device regulations, common technical documents and the progress made in implementation. HAVE AGREED as follows: ARTICLE 1 GENERAL PROVISIONS (1) Each Member State shall undertake all necessary measures to ensure that only medical devices which conform to the provisions of this ASEAN Agreement on Medical Device Directive (hereinafter referred to as

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