ANNOUNCEMENT | Alentra PD to launch on October 13, 2026.

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CAPABILITY

Prototyping, Test Methods & Verification / Validation

Alentra PD builds and evaluates prototypes, develops test methods and fixtures, and supports verification and validation testing to generate the evidence needed to refine designs and demonstrate requirements are met.

Capability

Prototyping, Test Methods & Verification / Validation

Alentra PD builds and evaluates prototypes, develops test methods and fixtures, and supports verification and validation testing to generate the evidence needed to refine designs and demonstrate requirements are met.

PROTOTYPING, TEST METHODS & VERIFICATION / VALIDATION

Build, Test, Learn & Demonstrate

Testing turns design assumptions into evidence. Alentra PD combines prototyping, clinically relevant test methods, custom fixtures, and disciplined verification and validation work to evaluate performance, uncover issues, and support the next development milestone.

Start your project

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Prototype & Learn

Build and evaluate prototypes to explore performance, identify issues, and guide design refinement.

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Clinically Relevant Evaluation

Create bench, ex-vivo, or other clinically relevant evaluations when appropriate to the product and stage.

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Test Methods & Fixtures

Develop test methods and fixtures around the requirements, risks, and questions the program needs to address.

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Verification & Validation

Execute and document verification and validation testing to demonstrate that defined requirements and user needs are met.

PROTOTYPING & TESTING CAPABILITIES

From Prototype to Objective Evidence

The right test approach depends on what the team needs to learn or demonstrate. Alentra PD develops prototypes, methods, fixtures, and testing strategies around the requirements and risks of each program.

Build the right test for the requirement

Effective testing starts with a method that represents the requirement being evaluated. Alentra PD develops test methods and custom fixtures—including clinically relevant setups when needed—to generate meaningful, repeatable evidence.

Concept & Feasibility

Prototype Generation & Evaluation

Build and evaluate prototypes through iterative design-test cycles to understand performance and refine the solution.

Product Design

Bench & Clinically Relevant Testing

Use bench, ex-vivo, cadaver, animal, or simulated-use evaluations when appropriate to the question being studied.

Prototype & Test

Design Verification Testing

Test design outputs against documented specifications to demonstrate that defined requirements have been met.

Engineering

Design Validation Testing

Evaluate the finished design against user needs and intended use using an appropriate validation approach.

From concept through commercialization, explore the capabilities that move medical device programs forward.

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OUR PROCESS

A Structured path from question to evidence

Concept & Feasibility

1

Define Test Objectives

Identify the requirements, risks, and technical questions the work needs to address.

Product Design

2

Prototype & Prepare

Build prototypes or test articles that allow the team to evaluate the design and its performance.

DFM Review

3

Develop Methods & Fixtures

Create methods, procedures, and fixtures that represent the requirement or use condition being evaluated.

Prototype & Test

4

Execute Testing

Conduct the appropriate prototype, verification, or validation testing for the program stage.

Verify & Hand Off

5

Analyze & Document

Review the results, document the evidence, and use what was learned to support the next decision.

TESTING & COLLABORATION

Use evidence to guide the next decision

Alentra PD works with client teams, clinicians, specialists, and manufacturing partners to develop testing approaches that reflect the product, its intended use, and the technical questions that matter. Results then inform refinement, risk reduction, and next steps.

Device & Clinical Relevance

Relevant device & clinical expertise

Testing experience spans products and clinical applications where performance must be evaluated under demanding technical or clinically relevant conditions.

RFID & NFC

Catheter-Based & Endovascular Devices

Experience developing methods and sophisticated fixtures to evaluate catheter systems, materials, deployment, and performance.

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Micro Molding & Microfluidics

Endoscopic & Minimally Invasive Devices

Experience with iterative prototyping, mechanical evaluation, and verification and validation testing for minimally invasive instruments.

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Explore this expertise

3D Printing & Prototyping

Surgical & Robotic Devices

Experience using design-build-test iterations, ship testing, and cadaver evaluation to resolve complex surgical-product challenges.

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Explore this expertise

Sterilization Solutions

Single-Use Disposables & Diagnostics

Experience developing test methods, procedures, fixtures, verification testing, and test reports for diagnostic and single-use products.

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Explore this expertise

Need to prove the design performs?

Tell us what you need to learn or demonstrate, where the design stands, and what testing milestone your program is preparing for.

QUALITY & COMPLIANCE

Objective evidence for regulated development

Verification and validation turn requirements and user needs into documented evidence. Alentra PD supports this work with structured test methods, procedures, fixtures, testing, and reporting within a quality-managed development environment.

  • ISO 13485:2016 quality management system
    Quality systems support disciplined testing and documentation for regulated product development.
  • Risk & Test Planning
    Risk analysis and defined requirements help determine what needs to be tested and documented.
  • Test Methods & Documentation
    Methods, procedures, fixtures, and test reports create a documented record of how performance was evaluated.
  • Verification & Validation Evidence
    Verification demonstrates that documented specifications are met; validation evaluates whether the design meets user needs and intended use.

WHAT COMES NEXT

Related capabilities

medical devices

Product Development

Move designs through detailed engineering, risk management, documentation, and manufacturing preparation before formal testing milestones.

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Explore Product Development

medical devices

Early Concept & Feasibility

Explore concepts and evaluate early prototypes before a program advances into detailed development and formal testing.

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Explore Early Concept & Feasibility

medical devices

Quality & Regulatory Support

Connect testing activities with quality systems, design controls, documentation, and regulatory support.

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Explore Quality & Regulatory

medical devices

Contract Manufacturing

Produce early and low-to-mid-volume units for verification and validation testing, clinical studies, and market launch.

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Explore Contract Manufacturing

Let's build the evidence your program needs

Share your current design stage, test objectives, and upcoming milestones with the Alentra PD team to discuss the right prototyping and testing approach.