Specialised in providing top-tier MedTech engineering solutions. The company is dedicated to guiding complex medical technology projects from concept to completion, ensuring unmatched efficiency, clear communication, and strategic risk management throughout the process.
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Perdigó understands that all users are crucial for developing effective medical devices. The organisation conducts in-depth user research to understand the needs, preferences, and behaviours of all users.
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The company offers engineering design services tailored to the unique needs of the med-tech industry, with expertise spanning the entire product development lifecycle. T his ensures that innovations are brought to market with precision and efficiency.
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Hardware and firmware development ensure that your medical devices are not only reliable and eficient but also compliant with the highest industry standards, ranging from ultra-low- power devices to larger-scale electronic systems.
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Industrial design team specialises in crafting attractive, intuitive, and commercially successful products that meet the needs of end-users. With a user-centric design approach, the team invests time up front to identify and prioritise design challenges, ensuring that every decision is evidence-based.
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Prototypes play a critical role in the development of new medical devices. Different types are required, each fulfilling a distinct purpose in the design and development process.
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Perdigó designs bespoke test fixtures to meet the unique needs of each project, ensuring that tests are as accurate and relevant as possible. The team provides detailed test reports with actionable insights, helping clients make informed decisions during the development process.
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Perdigó conducts ISO 14971-compliant hazard identification, risk estimation, and risk-benefit analysis across the full device lifecycle, ensuring safety is built in from the earliest design decisions.
Our team designs microfluidic systems for diagnostic and lab-on-chip applications, covering channel geometry, material selection, bonding and fabrication process definition, and functional validation under representative use conditions.
Perdigó manages the full IEC 62304 software lifecycle for medical devices, covering software requirements specification, architecture design, implementation, unit and integration verification, and ongoing maintenance across all software safety classes.
Our team brings deep materials expertise to medical device development, selecting and evaluating the right materials for each device contact category, from polymers and metals to coatings and adhesives, with biological evaluation conducted in line with the ISO 10993 series.
Perdigó's IP team carries out freedom-to-operate analysis, patentability assessments, and filing strategy throughout the development process, helping clients identify and protect their innovations before competitors and before regulatory submissions expose them.
Perdigó builds a clear, evidence-driven regulatory pathway from the outset of development, covering classification and pathway definition, standards mapping, evidence and testing strategy, and design control structure for both the EU and US markets.