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Quality Assurance

We provide Quality Assurance services, leveraging CLEIO’s robust processes and ISO 13485 certified QMS to elevate product safety, reliability, and compliance from concept to commercialization.

From Concept to Compliance, With Quality at the Core of our Process

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Our Quality Assurance services ensure that your product meets the highest standards of performance, safety and compliance, whether it’s a connected consumer device, a complex industrial system, or an embedded software in a medical device.
At CLEIO, we embed quality in every stage of development, helping our clients accelerate timelines, reduce risks, and bring reliable, high-performing products to market.
Our ISO 13485 certification for medical device development reflects the strength and maturity of our Quality Management System. It demonstrates our ability to consistently apply structured and well-documented processes that drive overall product quality from concept to launch, especially for high-stakes, regulated environments like healthcare.

What We Do

Quality Management & Planning
Risk Management
Design Controls
Design Verification Testing
Change Management
Document Control
Manufacturing Transfer & Support
Regulatory Compliance (US, CAN, EU)
Standards Analysis
Design History File (DHF)
Device Master Records (DMR)

Our Quality Assurance Team Guides You Through Design and Development Activities

Partnering with CLEIO gives you expert guidance in planning design and development activities, ensuring alignment with industry standards and regulatory requirements.
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Planning and Defining Requirements

We ensure that every stage of the product design and development lifecycle is planned and executed according to the industry’s highest standards, starting with robust, quality-driven processes.
This means we apply state-of-the-art processes and practices to ensure product reliability, safety, and performance.

Documentation Management

Our team expertly manages the documentation of the design and development process, applying good documentation practices and ensuring all documents are accurate, comprehensive, and ready for regulatory review, streamlining approval processes.

Risk Management

We ensure that risk management activities are fully integrated into the design and development process, identifying potential risks early and implementing effective mitigation strategies. Using proven methodologies like FMEA, we help you avoid costly setbacks and ensure product or software reliability.

Design Verification

Design verification is part of our expertise. We rigorously verify that the design outputs meet the design inputs requirements to ensure that the final device functions as intended. Our design verification process includes comprehensive testing, reviews, and traceability to ensure the product is on the right track for regulatory approval.

Regulatory Strategy Support

Our experts provide guidance on regulatory compliance, helping to align product design and development with current standards, ensuring your product or software meets both local and international regulatory requirements.

Timeline Estimations

We estimate the efforts and time required to complete the activities, enabling precise forecasting to ensure that projects stay on schedule and within scope.

Our Integrated Design and Development Process is Driven by our Quality Assurance Team

From concept to market, our IDEALTM design and development process integrates all necessary design controls and best practices in project management.

This process includes design planning, user needs, design inputs, design outputs, design verification, design validation, design review, and design transfer activities.
The result of this approach is high-quality, production-ready products along with comprehensive project documentation.

We are ISO 13485-Certified for Medical Device Development

Our Quality Management System (QMS) complies with the requirements of ISO 13485:2016, the internationally recognized standard for medical device development. It ensures that we meet regulatory requirements while delivering safe, high-quality products.
This certification reflects the robustness and traceability of our processes, which are designed to streamline product development in the MedTech industry, enhance operational efficiency, accelerate timelines, and reduce costs.
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Why Choose CLEIO for Your Software Development?

When you choose CLEIO, you’re choosing a dedicated partner who brings deep expertise, creativity, and precision to every software project. We build smart, scalable, and user-focused solutions that elevate experiences, drive results, and help you stand out in a competitive digital landscape.
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Enhanced Product Safety

Ensures that products or softwares are free from defects and operate safely, improving the user experience and reducing the risk of harm

Regulatory Compliance

Facilitates adherence to stringent regulatory standards, helping avoid legal issues and facilitating smoother market entry.

Faster Time-to-Market

By integrating quality assurance early and throughout the development process, potential issues are identified and resolved proactively—reducing delays, speeding up approvals, and enabling a smoother, faster product launch.

Improved Product Reliability

Increases the reliability, security, and performance of products, leading to higher customer satisfaction and trust.

Market & Investor's Confidence

Builds confidence among stakeholders, including users, partners, and investors, by consistently delivering high-quality products.

Streamlined Production

Enhances manufacturing processes, reducing waste and increasing efficiency through systematic quality control measures.

Long-term Profitability

Contributes to long-term profitability through the development of superior and competitive products that meet both market expectations and user needs.

Cost Efficiency

Minimizes costly recalls and legal suits by identifying and correcting issues before products reach the market.

Brand Reputation

Strengthens brand reputation by upholding high standards in product quality and user safety.

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