Medical Device Client

How a National Retailer Eliminated Tens of Thousands of Hours of Annual Manual Work Through Intelligent Automation

Challenge:

Time & Labor Consuming Mandatory Medical Device Reporting

FDA requires client to internally investigate and report any medical device-related adverse events and product problems.

Prior to automation, manual process took 1 to 2 weeks and 12 employees.

First team pulls complaint reports and reviews the customer complaint

Second team Manually locate device by lot numbers

Third team investigates and sends confirmation reports

Solution: Futran’s IPA Expertise

Bots were developed
to automate these
manual processes.

Bot will print daily
reports with the
location of the
devices within minutes.

Benefits:

Client saved $1.2m annually in labor spend

10 days : 2 hours

Services

AI & Automation

Digital Engineering

Business Process Operations

Industries

Financial Services

Life Sciences & Healthcare

Public & Social Impact

Resources

Company

Government (Contracts)

Services

AI & Automation

Digital Engineering

Business Process Operations

Industries

Financial Services

Life Sciences & Healthcare

Public & Social Impact

Resources

Company

Government (Contracts)

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We do not discriminate based on race, color, religion, sex, national origin, age, disability, veteran status, or any other legally protected status.