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11月份EDQM對(duì)CEP申請(qǐng)的電子遞交的路線圖進(jìn)行了修訂(附原文節(jié)譯)
1月份EDQM對(duì)CEP申請(qǐng)的電子遞交的路線圖進(jìn)行了修訂,其中的關(guān)鍵信息總結(jié)如下:
 
新的CEP申請(qǐng):從2018年1月1日起強(qiáng)制執(zhí)行eCTD。較之前發(fā)布指南規(guī)定的2017年1月1日推后了1年。
變更和續(xù)證:2018年1月起,不再接受PDF格式的電子遞交,只能采取eCTD或者是NeeS格式。
2020年1月以后,所有的遞交(新申請(qǐng),變更和換證)都必須采用eCTD格式。但是不包括TSE申請(qǐng),TSE申請(qǐng)仍可使用PDF格式。
2017年1月以后,不再接受Dropbox和CDs的遞交方式。只能使用CESP通道。
 
 
【原文】
 
Electronicsubmissions for CEP applications 
Revised Roadmap 2016-2020
 
1.Introduction 介紹
 
TheEDQM is the organisation responsible for the procedure of Certification ofSuitability to the monographs of the European Pharmacopoeia (CEP), andtherefore receives dossiers describing the manufacture and quality control ofsubstances for pharmaceutical use. 
TheEDQM has been encouraging the submission of applications in electronic formatsince 2007 and has provided regularly updated guidance for preparing andsubmitting eSubmissions (EDQM Guidance for electronic and paper submissions forCertificates of Suitability applications, PA/PH/CEP (09) 108). 
ThiseSubmission Roadmap aims at developing and improving the current processes forsubmission of electronic data related to CEP applications. The main goals areto have: 
Efficient and secure electronic handling of data related to CEP applications(submission, reception, validation, processing) 
Fully electronic processing without paper or any physical media 
Automation of data transfer and storage 
Alignment with practice in place in regulatory agencies for eSubmission ofmarketing authorisation applications.
TheRoadmap has been revised to align with the European procedures. 
 
2.Current situation 現(xiàn)狀
 
Proceduresfor the electronic submission of CEP applications have been in place since2007. The number of eSubmissions has increased regularly, however paperapplications, which are still accepted currently, represent about 10% ofapplications received. 
Withregards electronic formats, the EDQM has so far accepted several kinds offormats, pdf, NeeS1and eCTD, as described in the last version ofthe respective EDQM guideline. The majority of applications received are inpdf, which is the most basic electronic format. eCTD represent less than 20% ofthe formats received, regardless of the kind of submission (new application orrevision). 
TheEDQM has decided to use the CESP (Common Electronic Submission Platform) as thepreferred way to receive eSubmissions. However, currently the Dropbox remainsthe transfer system most used by applicants. 
3.Goals 目標(biāo)
 
Thissection describes the objectives to reach within the next years.
 
Topic 
Objectives 
Submission  format 
Single  format for submission of data: eCTD (except for TSE only submissions and for  submissions for substances for veterinary use only2). 
For  TSE only submissions, PDF continues to be standard format accepted. 
Submission  media and mechanisms 
Single  and secure entry point for eSubmission of data: CESP, or alternatively an  EDQM dedicated portal 
Application  form 
Implement  eApplication form/upload of electronic information from Application form 
Content  
Consistent  information, aligned with eCTD specification 
Receipt  and validation of data 
Automation  of data transfer and storage, reduction of manual handling and checks 
Use  by assessors 
Full  use of review tool for all kinds of applications 
 
4.Actions and Timetable 行動(dòng)和時(shí)間表
 
Thissection describes the detailed actions and estimated timeframes for completionof these actions in order to achieve the objectives described above and whichhave an impact on the preparation of the submissions by applicants.
 
Topic 
Timeframe 
Actions 
Submission   format and content
June 2016 
No further  acceptance of paper submissions for any kind of application (including TSE  only submissions) 
January  2018
Require  eCTD submissions for new applications (except for TSE only submissions and  for submissions for substances for veterinary use only3). 
For TSE  only submissions PDF continues to be standard format accepted. 
January  2018
Stop  accepting PDF submissions for revisions and renewals. Therefore, all such  submissions need to be in NeeS or eCTD format (except for TSE only  submissions and for submissions for substances for veterinary use only3). 
For TSE  only submissions PDF continues to be standard format accepted. 
January  2020
Require  eCTD submissions for all applications including requests for revisions and  renewals (except for TSE only submissions and for submissions for substances  for veterinary use only3). 
For TSE  only submissions PDF continues to be standard format accepted. 
Submission  media and mechanisms 
January  2017 
Stop the  use of the Dropbox and CDs, and use only the CESP (Common European Submission  Portal) 
 
主題
時(shí)間點(diǎn)
活動(dòng)
遞交格式和內(nèi)容
2016年6月
不再接受任何紙質(zhì)格式遞交(包括TSE申請(qǐng))
2018年1月
新的申請(qǐng)強(qiáng)制要求eCTD格式(不包括單獨(dú)的TSE申請(qǐng)和僅作為獸用的物質(zhì)申請(qǐng))
單獨(dú)的TSE申請(qǐng),標(biāo)準(zhǔn)的申報(bào)格式仍為PDF格式。
僅作為獸用的物質(zhì)申請(qǐng),可接受的格式為VNeeS格式。
2018年1月
變更和續(xù)證不再接受PDF格式。因此所有的此類(lèi)申請(qǐng)需要采用NeeS或者eCTD格式。(不包括單獨(dú)的TSE申請(qǐng)和僅作為獸用的物質(zhì)申請(qǐng))單獨(dú)的TSE申請(qǐng),標(biāo)準(zhǔn)的申報(bào)格式仍為PDF格式。
僅作為獸用的物質(zhì)申請(qǐng),可接受的格式為VNeeS格式。
2020年1月
所有的遞交(新申請(qǐng),變更和換證)都必須采用eCTD格式。(不包括單獨(dú)的TSE申請(qǐng)和僅作為獸用的物質(zhì)申請(qǐng))
單獨(dú)的TSE申請(qǐng),標(biāo)準(zhǔn)的申報(bào)格式仍為PDF格式。
僅作為獸用的物質(zhì)申請(qǐng),可接受的格式為VNeeS格式。
遞交媒介和機(jī)制
2017年1月
不再接受Dropbox通道和CDs方式的遞交。
只接受CESP通道的遞交方式。
 
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