Electronic Submissions (esubmissions) via EMA Gateway Webclient. An agency of the European Union

Similar documents
Submissions to the PSUR Repository using EMA Gateway/Web Client

esubmission Gateway and Web Client Training on the use of XML delivery files for Veterinary submissions

PSUR Repository Interactive Q&A

esubmission Gateway Web Client

EMA esubmission Gateway and Web Client: Questions and answers on Veterinary Applications

How to send submissions via the Web Client

The WIN applies to the Vet Applications team in the Veterinary Regulatory and Organisational Support service (V-VM-ROS).

Variations in ectd format Q&A document

ANSM 11/ Page 1 sur 6

Work instructions for US-FDA ANDA Submissions Work Instructions for ectd US-FDA ANDA Submissions

MEDICINES CONTROL COUNCIL

Use of CESP to submit electronic documents to EDQM

PSUR Repository and the EU single assessment

EMA Common Repository: Questions and answers relating to practical and technical aspects of the implementation

FINRA - AEP S TOCK R ECORD D ATA F ILE S UBMISSION Q UICK R EFERENCE G UIDE

US Food and Drug Administration. Revision History

MiFID II Transaction Reporting. Technical Specification

Get ready for ectd in South Africa. Current status at MCC

ectd Practical experiences of the ectd pilot project and way forward

esubmissions Web UI Release Notes

esubmissions Web UI Release Notes

Criteria Webinar. 13 th July European Update on Validation of ectd & NeeS submissions, July 2012

User Guidance for National Competent Authorities for PSUR Repository

Guidance for electronic and paper submissions for Certificates of Suitability (CEP) applications

PSUR Repository Implementation Plan

Transaction Reporting under Regulation 600/2014 ( MiFIR ) Operational and Technical Arrangements Central Bank of Ireland

Release Notes for TIGes ectd Guidance Comparison of version 2.0 with 1.0

SFT User Manual C:D. Secure File Transfer with Connect:Direct. Document date: 15 November 2016 Classification: Open Version: 4.0

EU Module 1 v1.4 Release Notes August 2009

Manuscriptorium for Candidates (M-Can) Help.

Session 4. Workshop on the implementation of ISO standard for ICSRs. Testing with EMA new process

How to upload documentation

Transaction Reporting under Regulation 600/2014 ( MiFIR ) Operational and Technical Arrangements Central Bank of Ireland

Annex IX: E-SUBMISSION THROUGH THE COMMON EUROPEAN PORTAL (CESP)

EudraVigilance support guide

EU Module 1 V3.0 Release Notes July 2015

Submitting High Quality ectd Submissions to FDA/OGD

Electronic World. Mag. Beate Gasser LCM/REUR. AGES Gespräch Wien, Österreichische Agentur für Gesundheit und Ernährungssicherheit GmbH

AFTN Terminal. Architecture Overview

X D I A L U P. X12 (HIPAA) Dial-up Transmission System. Document Version

Transfer Records to the State Archives with Exactly

IRIS Quick guide to the portal for Orphan Industry users

EUROPEAN ANTI-FRAUD OFFICE

REPORTING IN IMIS SYSTEM BENEFICIARY SEMINAR 20 MARCH 2018 SUBOTICA, SERBIA

IMMC v3 Communication protocol specifications

SEC COMPLIANCE ARCHIVE QUICK GUIDE (FOR IMAGESILO SUBSCRIBERS)

QUICK REFERENCE TO MDS 3.0 SUBMISSIONS, SUBMISSION STATUS, AND FINAL VALIDATION REPORTS

1. Document Control 2. Change Record Version Date Author(s) Comments 3. Reviewers Version Name Organisation 4. Distribution Version Date Name Status

Forms. GDPR for Zoho Forms

Preparing for FDA Mandated ectd Submissions

PROSPECT. FAQs for Applicants

Import Automation Engage

INSTRUCTIONS, CONDITIONS AND DISCLAIMER FOR THE SUBMISSION OF ELECTRONIC DOCUMENTS IN ILO S E-TENDERING SYSTEM

Guideline on the specifications for provision of an electronic submission (e-submission) for a veterinary medicinal product

e-submission Quick Reference Guide for Economic Operators

EudraCT release notes

Loan Closing Advisor SM. User Guide. December 2017

Container Status Messages

EudraVigilance Components & Functionality Introduction

KPLC SUPPLIER RELATIONSHIP MANAGEMENT USER GUIDE FOR VENDOR REGISTRATION, RFX PARTICIPATION AND PURCHASE ORDER COLLABORATION

EU Individual Case Safety Report (ICSR) 1 Implementation Guide

North Dakota Court System Frequently Asked Questions

Site User Guide. Oracle Health Sciences InForm CRF Submit Release Part Number:E

Change Control Process for European ectd Standards Version 1.1. December 2006

MiFID II Transaction Reporting. 29 September 2017

Parcel Data Exchange PDX Web Application Customer Guide

TRANSACTION REPORTING UNDER MiFIR: CNMV OPERATIONAL GUIDE

IRIS Quick guide to registration

PSD2 Major incident reporting 1 User Guidelines Document

File Upload Instructions Customer Access To Transcript Bulletin Publishing s FTP Site

Cover note on XEVMPD substance controlled vocabulary following the quality control exercise

ectd Next Major Version Business Requirements (11-JUN-09)

1 efilega Frequently Asked Questions

WFD Reporting Guidance 2016

User Guidance for submissions via esubmission Gateway / Web Client using xml delivery files

TRANSACTION REPORTING UNDER MiFIR: CNMV OPERATIONAL GUIDE

DATA SUBMISSION REQUIREMENTS MANUAL

Connectivity Implementation Guide

Regulatory Reporting Hub SFTP Connection How to connect via SFTP & upload Files

Gateway for Energy Marketers (GEM) User Guide for Gas Marketers

Regulatory Reporting Hub SFTP Connection How to connect via SFTP & upload Files

QUICK REFERENCE TO OASIS SUBMISSIONS, SUBMISSION STATUS, AND FINAL VALIDATION REPORTS

DEVELOPER GUIDE PART B CONNECTOR REQUIREMENTS

COMMISSION IMPLEMENTING DECISION (EU)

Secure File Transfer External User Guide. Guidance for 3 rd Party Recipients of Secure File Transfers from Lloyds Banking Group

Electronics Manufacturer e-submission Manual

IBM Sterling Data Synchronization Manager. User Guide. DocumentationDate:12October2012

e-frr SYSTEM USER GUIDE

New Single Form 2018 (offline) Quick Start Guide

Subject: Open letter on REMIT transaction reporting data quality

Pre-notification check for type IB Variations 1

ectd Next Major Release Business Requirements Collation (9-JUN-10) TOPIC Requirement Comment

ectd Next Major Release Business Requirements Collation (11 NOV 10) TOPIC Requirement Comment ICH Req No.

Common monitoring and information system Reporting in IMIS system

Guidance for electronic submissions for Certificates of Suitability (CEP) applications

Hewlett Packard Enterprise Smart Quote

ectd : Industry Experience

National Renal Administrator s Association Health Information Exchange. CROWNWeb Data Submission User s Guide

RMS & OMS Industry on-boarding to SPOR Webinar with Industry Change Liaisons

Web Portal Overview 1

Transcription:

Electronic Submissions (esubmissions) via EMA Gateway Webclient An agency of the European Union

The Gateway What is the Gateway? Gateway Options Key features of Webclient & Gateway (AS2/AS3) Overview of Gateway Set-up Registration Using the Webclient

What is the Gateway? An Agency-wide solution and central transmission point for accepting secure electronic regulatory submissions over the Internet. The EMA esubmission Gateway is a conduit, or "a route", along which submissions travel to reach their final destination. It does not open or review submissions; it automatically routes them to the relevant EMA Office. ectd Compliance check EMA Gateway (receives submission & sends MDN to sponsor)

esubmissions Gateway Options EMA Gateway Web Client Low cost option Uses applet EMA is using European Review System (EURS) to validate the ectd Submissions Gateway to Gateway (AS2) Applicability Statement 2 (AS2) and AS3 Gateway-to- Gateway Requires an AS2 & AS3 compliant gateway software EMA is using a product called Axway Synchrony Gateway Interchange (version 5.x) & EURS to validate the ectd submissions.

Feature comparison of WebClient and Gateway

Overview of Gateway Set-up Apply for Online Registration (Test & PROD simultaneously) Testing is strongly recommended for webclient users even though it is stated Optional when registering online.

EMA Gateway Webclient Facts EMA does not charge for the use of this solution ONE Webclient account is allowed per sponsor. A second account may be requested though please do provide a justification to esubregistration@ema.europa.eu Webclient uses Hypertext Transfer Protocol Secure (HTTPS) to ensure secure delivery of submissions over internet. Consultancy companies can register and send on behalf of Various sponsors.

Electronic Submissions Gateway Process What to do in order to use the gateway Determine the preferred route i.e. AS2/GW, or GW/Webclient To use the gateway webclient you need to ensure that online registration has been completed and account(s) have been activated. Understand and consult guidance documents on the esubmission website http://esubmission.emea.europa.eu/esubmission.html File naming convention described in the guidance document is followed correctly when uploading zip files.

Webclient Registration - 1

Webclient Registration - 2

Webclient Registration - 3

Webclient Registration - 4

Using The Webclient 1. Logon with the credentials supplied in communication from the registration team 2. Start Submitting! Always select the send documents more than 10MB option to use Large file applet, Note that receipts (MDN) are sent only when you use this option.

Key Points during the Webclient Transmission -1 There are two automated messages sent during the transmission: 1. Always use the Large File Applet for All transmissions via the webclient. 2. The Receipt is sent once the submission has been successfully received by the EMA gateway webclient. It is a simple text file with reception timestamp and is merely a receipt - this does not indicate a successful ectd technical validation. To note Receipt is sent only when using the Large File applet. 3. The final Acknowledgement is an xml file sent after the system has completed the ectd technical validation of the submission. It contains the result of the validation (SUCCESS or FAILURE). In case of a failure, a detailed description of the error is included in it. 4. Dependent on the submission size and webclient gateway queue, both automated messages can take anything between 5 mins ~ 4 hours for the delivery back to sponsor.

Key Points during the Webclient Transmission - 2 4. Where applicable, for multiple submissions, please trigger webclient transmission belonging to same product/dossier in sequential order. e.g. If sponsor needs to send 0033, 0035, 0036 for same product please send them in that order and allow some gap between those transmissions. Failure in following this may result in Negative ectd validation. 5. Webclient submissions should be archived as a zip file. The compressed application file must comply with the ZIP open format.

Key Points during Webclient Transmission - 3 Sponsor s Inbox view showing Acknowledgement and Receipt:

Acknowledgement Example

Filenaming Conventions for Webclient - 1 Effective from 15 th January 2013 please use following File Naming Convention for ALL submissions: Example: ESUBPXYZ_ESUBPROD_HC000999_Wonderpill_var-typeII_0020.zip

ectd Technical Validation Issues ectd Technical Validation identifies and rates the severity of the errors (P/F checks from the ectd criteria) encountered in a typical ectd submission, results are indicated in Final Acknowledgement message as SUCCESS or FAILURE. The ectd validation criteria for these are available here: http://esubmission.emea.europa.eu/tiges/tigesdocuments.html Duplicate Submission Typo in the product number (HC000xxx) If an already existing sequence (in EMA database) has been modified and sent to the agency as replacement! eu-regional.xml is corrupted OR is absent altogether Empty folder

How to Avoid Problems - 1 1. Correct Routing ID s should be used for respective environments and reflected correctly in the Submission s filename e.g. ESUBPXYZ_ESUBPROD_HC000999_Wonderpill_initial-maa_0020.zip 2. Incorrect folder structure used in Zipped file sent to EMA, Always ensure that Sequence Number(0xxx) folder is at the root, as reflected below:

How to Avoid Problems - 2 4. ectd submissions should be archived as a zip file. The compressed application file must comply with the ZIP open format. 5. Duplicate submissions - Once is Enough! - Webclient only processes the first submission not the duplicate. - If the first submission was in error, contact ectd support team at ectd@ema.europa.eu 6. Bad characters in the file names (NO Spaces!) only underscore is allowed to separate the filenames. No other special characters are allowed. 7. Do not send duplicate submissions using both CD or DVD and webclient.

Why should you bother? These errors require us to manually process your gateway submission Manually processed submissions delay access to your material More hands in the pot increases chances for error Sometimes these issues result in us rejecting your submission

Contact Information & Useful links Registration Documentation (contact info, forms, guidance documents): http://esubmission.emea.europa.eu/esubmission.html Registration team: esubregistration@ema.europa.eu for Technical issues during webclient set-up: gatewaysupport@ema.europa.eu for ectd technical validation issues (negative Acknowledgements): ectd@ema.europa.eu TIGes Guidance on ectd s - this guidance document also contains required links to all submission types:http://esubmission.emea.europa.eu/tiges/docs/ectd%20guidance%20 Document%202%200_2011_TIGes%20adoped%20for%20publication.pdf

Thank You for your interest! Questions?