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5 Reasons to choose the EXTEDOsuite for Regulatory Information ...

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Products within <strong>the</strong> <strong>EXTEDOsuite</strong><br />

Registration<br />

Management<br />

Submission Viewing<br />

& Reviewing<br />

MPDmanager<br />

MPDmanager is EXTEDO’s comprehensive<br />

XEVMPD data base system<br />

and <strong>the</strong> integral part of <strong>the</strong> <strong>EXTEDOsuite</strong>.<br />

It provides <strong>the</strong> functionality of a central<br />

product data reposi<strong>to</strong>ry and enables you<br />

<strong>to</strong> manage and maintain XEVMPD data<br />

efficiently and in compliance with current<br />

regula<strong>to</strong>ry requirements.<br />

MPDviewer<br />

MPDviewer is a free of charge<br />

web based application. It enables you <strong>to</strong><br />

get your XEVMPD data records back from<br />

EVWEB, evaluate data, and generate reports.<br />

Submission Management<br />

& Publishing<br />

eCTDmanager<br />

eCTDmanager enables you <strong>to</strong><br />

build, view, validate and publish compliant<br />

submissions based on CTD, eCTD, NeeS,<br />

eCopy, IMPD, CTA, VNeeS, DMF, ASMF<br />

and o<strong>the</strong>r submission structures easily.<br />

PlantOS<br />

EXTEDO PlantOS 3 is an off-<strong>the</strong>shelf<br />

solution <strong>for</strong> regula<strong>to</strong>ry affairs in Crop<br />

Sciences that manages <strong>the</strong> assembly and<br />

compilation of electronic dossiers. The<br />

standards e-PRISM (USA) e-Index (CAN)<br />

CADDY.xml (EU) are supported.<br />

Submission<br />

Validation<br />

EURSvalida<strong>to</strong>r<br />

EURSvalida<strong>to</strong>r supports you in<br />

validating medicinal and veterinary eSubmissions.<br />

The valida<strong>to</strong>r is used by <strong>the</strong><br />

majority of European National Authorities<br />

including EMA <strong>to</strong> ensure eCTD and NEES<br />

compliance. EURSvalida<strong>to</strong>r is available in<br />

several versions with different functionality<br />

and validation sets.<br />

EURSvalida<strong>to</strong>r Global<br />

EURSvalida<strong>to</strong>r Global is an add-on<br />

<strong>for</strong> EURSvalida<strong>to</strong>r that provides enhanced<br />

functionality and additional validation sets.<br />

EURS<br />

EURS serves as a complete eCTD<br />

validation and reviewing software solution.<br />

It reports whe<strong>the</strong>r a submitted eCTD- or<br />

NeeS-based application con<strong>for</strong>ms <strong>to</strong> <strong>the</strong><br />

official <strong>for</strong>mat.<br />

Pharmacovigilance<br />

Management<br />

PcVmanager<br />

PcVmanager is a drug safety management<br />

software solution based on <strong>the</strong><br />

E2B and MedDRA industry data standards,<br />

that enables you <strong>to</strong> classify, create, review,<br />

submit, and maintain pharmacovigilance<br />

data and Adverse Event reports.<br />

DOCmanager<br />

DOCmanager is an add-on <strong>for</strong><br />

eCTDmanager that allows <strong>the</strong> creation and<br />

maintenance of many child dossiers based<br />

on one parent dossier and reduces update<br />

times <strong>for</strong> variations.<br />

RLPmanager<br />

RLPmanager is EXTEDO’s advanced<br />

solution <strong>for</strong> report level publishing;<br />

it has been designed <strong>to</strong> optimize prepublishing<br />

work and support clinical study<br />

departments in managing and preparing<br />

study reports by au<strong>to</strong>mated processes.<br />

RLPmanager provides <strong>the</strong> environment<br />

and functionality <strong>for</strong> creation, compilation,<br />

validation and publishing of clinical and<br />

nonclinical study reports that later become<br />

part of eCTD or NeeS submissions.<br />

About us<br />

EXTEDO is <strong>the</strong> key software and service<br />

solutions provider in <strong>the</strong> field of Regula<strong>to</strong>ry<br />

In<strong>for</strong>mation Management (RIM). EXTEDO’s<br />

focus is on optimizing clients’ eRegula<strong>to</strong>ry<br />

business processes. The company’s<br />

enabling technology, <strong>the</strong> <strong>EXTEDOsuite</strong>,<br />

is unique in that it covers <strong>the</strong> complete<br />

regula<strong>to</strong>ry landscape including: product<br />

registration planning & tracking (IDMP),<br />

submission management, pharmacovigilance<br />

management and document management.<br />

Today, EXTEDO serves over 700<br />

cus<strong>to</strong>mers in 60 countries, including <strong>the</strong><br />

EMA and more than 25 regula<strong>to</strong>ry authorities<br />

worldwide.<br />

www.extedo.com<br />

EXTEDO GmbH<br />

Einsteinstraße 30<br />

85521 Ot<strong>to</strong>brunn / GER<br />

Phone: +49 (89) 189454-0<br />

Fax: +49 (89) 189454-999<br />

EXTEDO, Inc.<br />

1235 Westlakes Dr., Suite 285<br />

Berwyn, PA 19312 / USA<br />

Phone: +1 (855) 328 3500<br />

Fax: +1 (610) 240 9301<br />

14/09<br />

E-mail: info@extedo.com<br />

Internet: www.extedo.com

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