Quickstart

These sections are all about getting set up to perform your search. They are simply forms to fill out in order to provide the information necessary for final report generations.

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Creating a Project

To initiate a new project, simply click ‘Create New Project’ from the Home Page

This will take you to a screen to enter the details about your project.

Creating a Device and a Company

If this is your first time running a project (or for a new Manufacturer, or new Device), you will need to create short profiles with the relevant information.

Fill out the following form fields:

Name: This is the name that will show up within the CiteMed.io app. It’s more of an identifier/internal name.

Short Name: This is the non-legal name of the manufacturer used in more casual references.

Long Name: The full legal entity name of the manufacturer.

Address: Manufacturer’s corporate address.

Logo: A logo image that will be automatically inserted into final Microsoft Word Document Deliverables

Field
Description

Name

This is the name that will show up within the CiteMed.io app. It’s more of an identifier/internal name.

Short Name:

This is the non-legal name of the manufacturer used in more casual references.

Long Name

The full legal entity name of the manufacturer.

Address

Manufacturer’s corporate address.

Logo

A logo image that will be automatically inserted into final Microsoft Word Document Deliverables

Select or Create a New Product/Device

The ‘Device’ is the target device for which you are performing the review. It is created with a basic form inside the ‘New Project’ page.

Field
Description

Device Name

The marketing (official) name of your device/product.

Manufacturer

You will select from a list of created Manufacturer profiles.

Classification

This is the risk classification of the device (IIa, III, A, B, C etc.)

Markets

An abbreviated line of markets where the product is sold (this is not required for reviews). ie. “EU, US, China”

Project Type

The project type has several options, most of which will not affect standard users (only enterprise).

Project
Description

Lit Review

Standard Review (most users should select this).

CER

Those using other CiteMed.io tools and performing Clinical Evaluation Reports can select this.

PMCF

If report is conducted as part of a Post Market Clinical Follow-up procedure, you can select this option.

Vigilance

If report is performed for vigilance or Post Market Surveillance purposes, select this option.

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