Performing standard summative usability evaluation

Standard Summative Usability Evaluation

Standard Summative Usability Evaluations use a templated plan to meet ISO 11607 Section 7 sterile packaging validation requirements.

 

Who is Standard Summative Usability Evaluation for?

Engineering teams for medical device manufacturers who want to be compliant with ISO 11607 but are budget-constrained often rely on standard summative evaluations of usability.

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What's Included in a Standard Summative Usability Evaluation?

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Meets ISO 11607 Section 7 Requirements

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Templated project plan

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Standard evaluations occur once a quarter

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One package tested only

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15 end users

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Photography of aseptic presentation techniques for clients’ products

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Video and audio recording of the entire process of the study

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Preliminary meeting about acceptance criteria for packaging

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Clinical assessor profile(s)

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Details of the use environment, gowning, and surgical suite simulation

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Objective evidence that the three items required by ISO 11607-01:2019 have been evaluated

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Protocol report

I have had the opportunity to work with Matt Terbush and his team on several Usability Evaluations over the past three years during my time with Coloplast and have nothing but good things to say about this offering from PCL.

Chris Kelley
R&D Packaging Engineer

Let's Start Your Usability Evaluation

To get started on your usability evaluation, please provide your contact information and select an option that fits your needs or select 'I Need Guidance' if you require some assistance.

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More Usability Evaluation Options

Usability Evaluation

Formative

Prior to usability evaluation, performing a formative study may be helpful in gaining feedback before a design freeze.

Usability Evaluation

Custom Summative

Custom Summative Usability Evaluations meet ISO 11607 sterile packaging validation requirements. The custom approach allows for additional feedback on labels, IFUs, and more.