Application & Website Development

Corporate Identity & Logo Design, Medical Technology, SEO and Content Marketing, Software Development, Strategy and Design, Web Development

About the Project

CarePoint Solutions wanted to offer a streamlined, automated method of creating a Quality Control plan for medical diagnostics, to help hospitals and laboratories avoid errors — one of the leading preventable causes of death in healthcare settings.

Challenges

  • Help the client to define customer profile, understand their problems, needs, and behaviors related to their quality control and regulatory compliance needs

  • Create simple UI that will help users to have a positive experience with the product

  • Create a marketing website which looks and works seamlessly across different devices and platforms

  • Design product purchase and activation process

  • Design and create account portal user interface that looks and works seamlessly across different devices and platforms with the user in mind in the first place (user-centric design)

  • Deliver report information in easy to understand visual representation

  • Create the possibility for the user to easily access their report on any device at any time

  • Give user actionable information that he can access at any time at any device

Research

  • Stakeholder interviews
  • User interviews
  • Competitor analysis

UX

  • Development of customer/user personas
  • User journey map
  • Wireframing
  • Prototyping

UI

  • Screen designs
  • User Guide
  • Creating assets for development

Where does the PRO-QCP step in?

PRO-QCP is quality assessment procedure software which helps clients to get their Risk Assessment Report which is mandatory for acquiring the CLIA Certification for their devices in their families. By CLIA Certification rules, each facility and it’s equipment has own device which are used. These devices are usually multiplied over departments and facilities This means that every single facility and department has to have each of their devices CLIA certified individually.
In order to make that possible facilities must generate Risk Assessment Report that is made by Device’s Module which can be bought in PRO-QCP Device Modules Shop for every single device and assigned to it through PRO-QCP client’s dashboard. These modules help facilities to generate reports quickly and achieve CLIA Certification Number. Process is simple it guides user through all necessary things intuitively. Each device Risk Assessment process takes several minutes to be done and generated.

Facility

Department

Devices

Risk Assesment Report

Device Risk Assesment

Device Modules Shop

Device Modules Shop

Device Risk Assesment

Risk Assesment Report

CLIA Licence

User Experience

Registration / Login

Add / Manage Locations

Buy / Manage Modules

Risk Assesment Report

Quality Checklist

Risk Assesment

Suggestion Report

Process repetition for every single module and for every single facility and department

01

Login

Existing users will be prompted directly to the dashboard from where they can manage locations (facilities and departments), modules etc.

Unregistered users will be required to buy a module and then fill out the registration form with legal details and to setup locations information then will be able to access the dashboard screen and other screens.

02

Locations

Once user setup an account and log in into dashboard he will be able to manage and add locations (facilities) and departments.

These are the main factor for Risk Assesment Modules which will be registered to specific department and facility and they can be used only once per module.

03

Modules

User is required to buy module per device which has to be assigned to a specific department and facility. Module can be used once per Device Risk Assessment.

PRO-QCP has integrated shop for modules which is easily accessible for user and once module is bought it will appear in dashboard as unassigned.

MODULES SHOP

04

Risk Assesment

PRO-QCP integrated Risk Assessment tab for every single module and it starts with Acceptability Matrix compares real results and determines if the risk is acceptable or not.

User fils out forms with noticed risk and their repeating frequency, together with acceptance criteria.

These details are used in generating Risk Assessment Report.

05

Quality Checklist

Quality Checklist is addition to report which should confirm all the steps user took to ensure that Risk Assessment is not completed propperly.

06

IQCP Report

Once user setup an account and log in into dashboard he will be able to manage and add locations (facilities) and departments.

These are the main factor for Risk Assessment Modules which will be registered to specific department and facility and they can be used only once per module.

07

Suggestion Report

User can download and print suggestion report which should help him to reduce risk and to improve overall device usage quality in his facilities and departments.

Suggestion reports are printed and then written by hand by directors or HRs personally.

THANK YOU!

Give us a call

Your content goes here. Edit or remove this text inline or in the module Content settings.

Phone call:

CALL US AT: 718-858-8858

Schedule a Meeting

Your content goes here. Edit or remove this text inline or in the module Content settings.

Pick date and time:

SCHEDULE NOW