Custom configuration in meddevo

Add a Product Group (PG) manually

Favorites

eTD Portfolio Import via Excel

Document Import in meddevo

Import of (External) Documents

Create a Document with the meddevo Writer

Document Monitoring Overview

Scope: Are other Referenced Entries (e.g. Products ) automatically included?

Update a monitored Document

Regulatory Frameworks/Regulatory Focus quick Selection

Import Excel Data into a Collection

Workflow Templates

Create a new User

Create new Inspections

Report of a Data Import

Audit Trail Overview

Bulk Changes - multi editing

Inspector Overview

Form Field Information

Copy an Entry

Include Scopes in new Documents

Assign a Company Role to a User

Learn about Company Roles

User Interface Overview

Semantic Versioning meddevo Web App

User Profile

meddevo Helpdesk Overview

meddevo Structure Overview

REST API - Documentation of meddevo

Connections Overview

When is a Document up to date and when is it outdated?

Add Documents to a Submission

Create a Submission

Submission Monitoring

REST API

Creation of Company Roles

Create an Entry in the Applicable Requirements Collection

Submission Download

Create an Entry in the Regulatory Requirements Collection

Submissions Overview

How to create a List of Applied Standards (LoAS) for eTD

Add a Product (P) manually

Add Technical Documentation (eTD) manually

Add Products (P) via Excel Import

Document based vs content based

Folder Preview Overview of the current Technical Documentation (Documents)

Creation of Folder Preview Templates

Creation of CEP & CER based on a Writer Template

How to set up meddevo for your portfolio

Clinical Evaluation Management - Overview

Microsoft Excel - Character Limit

Information is missing in documents

Supported Browsers in meddevo

Approve Word-Documents in meddevo

Create a new meddevo Writer Document Template

Add Product Groups (PG) via Excel Import

Add Technical Documentations (eTD) via Excel Import

How to create a List of Applied Standards (LoAS) for Product Groups

Applicable Requirements/Regulatory Requirements - Overview (Standard Management 2.0) 

Name field in the Collection Management

What content is monitored in meddevo Writer documents?

Basic Functions Videos

Regulatory Updates 2025

Admin Training/Key User Training - Videos

meddevo does not have an offline mode

Review and Approval Workflows in meddevo

Multi-Language Use in meddevo & Language Settings

How to export a document

How to export your data

How to export a technical documentation

Date/Time Format

DeepL API - Automated Translation in meddevo

Access Control Management 

Best place to learn navigation and general handling.

Getting started

User Interface

Creation and Import of Entries

What regulatory aspects matter most in the beginning

Regulatory Startpoint

FAQs

Here you will find everything you need to know about handling documents.

Documents

Document Monitoring

Document Scope

Entries

Instructions and information on importing and exporting.

Import & Export

How the audit trail works is explained here.

Audit Trail

Inspections

Folder Preview

Connections

Here we take a closer look at the administration area and the features it contains.

Administration

User Management

An overview of all changes resulting from updates to the software.

2024

2023

2022

Regulatory Processes

How to manage standards and guidances and automate documents

Standard Management

Submissions

Clinical Evaluation

An overview of all changes resulting from updates to the software and standard updates.

Regulatory Updates

2025

Short videos with specific training content

meddevo Trainings Videos

Basic Functions

Administrator/Key User

meddevo Writer

<figure class="media"><div data-oembed-url="https://vimeo.com/1060081739"><div style="position: relative; padding-bottom: 100%; height: 0; padding-bottom: 56.2493%;"><iframe src="https://player.vimeo.com/video/1060081739" style="position: absolute; width: 100%; height: 100%; top: 0; left: 0;" frameborder="0" webkitallowfullscreen="" mozallowfullscreen="" allowfullscreen=""></iframe></div></div></figure><p>With the new selection of the Regulatory Frameworks via a dropdown menu <strong>(1)</strong>, it is possible to determine the Regulatory Focus for the entire application.<br>After the selection, the collection entry views, inspections and the folder preview for the selected regulatory framework are displayed.</p><figure class="image"><img src="https://dytab.github.io/user-manual/regulatory-framework/quick-selection-en.png"></figure><p>&nbsp;</p><p><br><strong>Search supported Keywords:</strong><br><strong>- Regulatorischer Fokus</strong><br>&nbsp;</p>

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