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俄羅斯聯(lián)邦藥品注冊(cè) -Registration of medicines in the Russian Federation

Регистрация лекарственных средств в РФ

在進(jìn)入俄羅斯聯(lián)邦醫(yī)藥市場(chǎng)之前，每種藥品都必須經(jīng)過(guò)注冊(cè)程序。 

Before entering the pharmaceutical market of the Russian Federation, every medicinal product must undergo the registration procedure.

在國(guó)外和俄羅斯生產(chǎn)的藥品都必須進(jìn)行國(guó)家注冊(cè)。 

State registration is required for medicines manufactured both abroad and in Russia.

該程序確認(rèn)藥品的質(zhì)量、療效和安全性。

This procedure confirms the quality, effectiveness and safety of the drug.

形成注冊(cè)檔案 Formation of the registration dossier

形成注冊(cè)檔案 Verification of documentation

專業(yè)知識(shí) Expertise

納入注冊(cè) Inclusion in the register

俄羅斯國(guó)家藥品注冊(cè)-State registration of medicines

俄羅斯國(guó)家藥品注冊(cè)是對(duì)藥品進(jìn)行檢驗(yàn)并授權(quán)其在我國(guó)銷售和用于醫(yī)療目的的過(guò)程。 Is the process by which medicines are tested and authorised for sale and use for medical purposes in our country.

在俄羅斯聯(lián)邦注冊(cè)藥品是一項(xiàng)相當(dāng)復(fù)雜的程序，要求申請(qǐng)人做好充分準(zhǔn)備，包括臨床試驗(yàn)，并提交大量文件。這可能需要很長(zhǎng)的時(shí)間和大量的資金投入。

Registration of a medicinal product in the Russian Federation, being a rather complex procedure, requires the applicant to make thorough preparations, including clinical trials, and to submit a large amount of documentation. It can take a long time and require significant financial outlays.

為了避免被俄羅斯國(guó)家機(jī)構(gòu)拒絕的風(fēng)險(xiǎn)，并順利地在俄羅斯聯(lián)邦注冊(cè)醫(yī)藥產(chǎn)品，請(qǐng)聯(lián)系我們的注冊(cè)專家。我們將在您的醫(yī)藥產(chǎn)品進(jìn)行國(guó)家注冊(cè)的各個(gè)階段提供專家協(xié)助。

To avoid the risk of rejection by the state authority and to register a medicinal product in the Russian Federation without problems, contact the specialists of shanghai SEC. We provide expert assistance at all stages of state registration of your medicinal product.

根據(jù)歐亞經(jīng)濟(jì)聯(lián)盟（EAEU）標(biāo)準(zhǔn)

According to EAEU standards

歐亞經(jīng)濟(jì)委員會(huì)理事會(huì)已將根據(jù)國(guó)家規(guī)則進(jìn)行注冊(cè)的可能性延長(zhǎng)至2023年12月31日。

The Council of the Eurasian Economic Commission has extended the possibility of registration under national rules until 31 December 2023.

根據(jù)俄羅斯國(guó)家標(biāo)準(zhǔn)注冊(cè)

According to the national standard

我們支持俄羅斯制造商在2023年12月30日前提交藥品注冊(cè)可享受 10% 的折扣。如果您還有任何疑問(wèn)，請(qǐng)隨時(shí)與我們聯(lián)系--我們將親自為您解答。

We support Russian manufacturers and offer a 10% discount on registration until 30 December 2023. If you still have any questions, please do not hesitate to contact us - we will answer you personally.

須注冊(cè)的藥品種類：

Categories of medicines subject to registration:

首次出現(xiàn)在俄羅斯市場(chǎng)上的藥品；

drugs that first appeared on the Russian market

已在俄羅斯聯(lián)邦注冊(cè)，但改變了包裝、劑量、名稱等的藥品；

drugs already registered in the Russian Federation, but changed their packaging, dosage, name, etc.

制劑，其化學(xué)成分已被至少一種成分改變；

preparations, the chemical composition of which has been changed by at least 1 component。

俄羅斯藥品注冊(cè)的各個(gè)階段

Stages of drug registration

1.形成藥品注冊(cè)檔案并提交俄羅斯衛(wèi)生部-Formation of the registration dossier and its submission to the Ministry of Health of Russia;

2.核實(shí)文件并獲得專家審查授權(quán)-Verification of documentation and obtaining authorisation for expert review

3.檢查質(zhì)量，檢查藥品預(yù)期收益與潛在風(fēng)險(xiǎn)的比例-Examination of quality and examination of the ratio of the expected benefit to the potential risk of using the medicine;

4.決定俄羅斯藥品注冊(cè)、將其列入俄羅斯醫(yī)藥產(chǎn)品注冊(cè)登記冊(cè)并頒發(fā)注冊(cè)證書-Decision on registration of the drug, its inclusion in the register of medicinal products and issuance of a registration certificate

藥品注冊(cè)截止日期

Registration deadlines

自繳費(fèi)和提交所需文件之日起30個(gè)日歷日內(nèi)頒發(fā)俄羅斯藥品證書。

The certificate is issued within 30 calendar days from the date of payment of the fee and submission of the required documents.

藥品注冊(cè)證書本身的有效期為無(wú)限期。

The validity of the certificate itself is not limited.

海關(guān)聯(lián)盟EAC認(rèn)證中心/上海經(jīng)合工業(yè)設(shè)備檢測(cè)有限公司

公司地址：上海浦東新區(qū)高科東路777弄1號(hào)樓2017室

聯(lián)系我們：上海經(jīng)合工業(yè)設(shè)備檢測(cè)有限公司/俄羅斯EAC證機(jī)構(gòu)中國(guó)代表處
電話：021-36411223   36411293
郵件：eac@cu-tr.org 
手機(jī)微信：18621862553