Testing Services for Your
Product Market Entry
Every product undergoes rigorous compliance testing for performance, safety, security and usability before it can enter a regulated market. NexorTest is your single accredited testing partner for EMC/EMI, environmental, reliability, medical device cybersecurity, and usability/human factors testing covering MedTech, Automotive, Telecom, Defence/Aerospace, Railway and Commercial products under one roof, with compliance reports delivered in as little as 72 hours.
One Partner. Every Compliance Test Your Product Needs
From electromagnetic performance to real world reliability, digital security and human factors. NexorTest covers every test your product needs before it can be certified and sold.
EMC/EMI Testing
Pre-compliance and compliance testing in 1m & 3m semi anechoic chambers (30Hz- 40GHz), ANSI C63.4 compliant, for Commercial, Automotive, Telecom, Medical, Railway and Defence/Aerospace products.
- Emissions
- Immunity
- ANSI C63.4
Environmental Testing
Climatic simulation, dynamic & vibration, ingress protection, aircraft electrical, optical fiber, telecom interface, connector and electrical safety testing under real world operating stress.
- Climatic
- Vibration
- IP Rating
Cybersecurity Testing
VAPT, SBOM generation, threat modeling and submission ready cybersecurity documentation for medical devices from connected Class II hardware to AI powered SaMD.
- VAPT
- SBOM
- IEC 81001-5-1
Usability Testing
- IEC 62366
- FDA HFE
- UX Research
Why test before you certify
Regulators increasingly refuse incomplete submissions outright. Since October 2023, the FDA can refuse to accept premarket submissions for “cyber devices” that lack SBOM, threat modeling and penetration testing evidence. EU MDR Notified Bodies are routinely requesting IEC 81001-5-1 evidence for software heavy devices, and missing usability documentation is a common cause of Additional Information Requests. Testing early not at the point of submission, alongside your medical device design and regulatory certification plan is what keeps a product on schedule. This is especially true for Software as a Medical Device (SaMD), where cybersecurity and usability evidence are now reviewed together.
EMC/EMI Testing Solutions for Your Product Needs
What is EMC/EMI testing? EMC (electromagnetic compatibility) and EMI (electromagnetic interference) testing verifies that a product neither emits excessive electromagnetic energy nor malfunctions when exposed to it from nearby devices. It is a mandatory step for market certification (CE, FCC, BIS and more) across commercial, automotive, telecom, medical, railway and defence/aerospace products, and NexorTest delivers results in ISO/IEC 17025 accredited chambers within 72 hours.
Want the full details on our EMC/EMI testing capabilities?
Environmental Testing Solutions for Your Product Needs
Climatic simulation, vibration, contamination, ingress protection, aircraft electrical and telecom interface testing to ensure product reliability and safety.
What is environmental testing? Environmental testing subjects a product to simulated real world conditions temperature extremes, humidity, vibration, shock, dust and water ingress, corrosion and more to confirm it will keep working reliably throughout its operating life. Standards such as MIL-STD-810, IEC 60068 and BS EN 60529 (IP rating) define the exact test parameters expected by regulators and OEM customers.
Cybersecurity Evidence Regulators Demand
Since October 2023, the FDA can refuse premarket submissions for “cyber devices” lacking cybersecurity documentation. NexorTest delivers every element regulators require.
What is medical device cybersecurity testing? It is the process of assessing a connected or software driven medical device for exploitable vulnerabilities through penetration testing (VAPT), threat modeling and a Software Bill of Materials (SBOM) and compiling the documentation FDA and EU MDR reviewers require. Any device with software and a digital interface, including USB, Bluetooth or Wi-Fi, is likely in scope under the FDA 2023 cyber device guidance and IEC 81001-5-1.
Want the full details on our cybersecurity testing capabilities?
Usability Testing Services for Global Markets
Expert usability studies, UX research and human factors evaluation across the US, EU, India and worldwide – meeting IEC 62366 and FDA Human Factors requirements.
What is usability testing? Usability testing observes representative users interacting with a product to identify use errors, confusion points and safety risks before and after launch. For medical devices, IEC 62366 and FDA Human Factors guidance require both formative evaluation (iterative, during design) and summative evaluation (a final validation study, typically with 15-25 participants per user group) before regulatory submission.
Find the Right Test for Your Product
A quick side-by-side of standards, timelines and deliverables across our four testing disciplines.
| Testing Type | Primary Standards | Typical Timeline | Key Deliverable | Best For |
|---|---|---|---|---|
| EMC/EMI Testing | IEC 61000, CISPR, MIL-STD-461 | 3-10 days per config | Compliance Test Report (72 hrs) | Commercial, Automotive, Medical, Defence |
| Environmental Testing | MIL-STD-810, IEC 60068, BS EN 60529 | 1-4 weeks | Environmental Test Report + IP Rating | All hardware products |
| Cybersecurity Testing | FDA 2023 Guidance, IEC 81001-5-1, AAMI TIR57 | 4-6 weeks | VAPT Report + SBOM + Threat Model | Connected medical devices, SaMD |
| Usability Testing | IEC 62366, FDA Human Factors | 2-4 months (summative) | HFE Report / Usability Engineering File | Medical devices, IVDs, healthcare software |
Testing Across Every Regulated Sector
From connected medical devices and SaMD to industrial IoT and defence systems, our specialists deliver testing tailored to how each sector actually operates.
Testing Services Questions Answered
Common questions across our EMC/EMI, environmental, cybersecurity and usability testing services.
What is EMC/EMI testing and why is it required?
EMC (electromagnetic compatibility) and EMI (electromagnetic interference) testing verifies that an electronic product neither emits excessive electromagnetic energy nor is disrupted by electromagnetic energy from other devices. It is required for market certification in almost every jurisdiction, since uncontrolled interference can disrupt other equipment, including safety critical medical, aviation and telecom systems. NexorTest performs emissions and immunity testing in ISO/IEC 17025 accredited 1m and 3m semi anechoic chambers covering 30Hz-40GHz, ANSI C63.4 compliant, with compliance reports delivered within 72 hours.
How fast can I get EMC/EMI compliance reports?
The NexorTest ISO/IEC 17025 accredited lab, equipped with 1m & 3m semi anechoic chambers (30Hz-40GHz, ANSI C63.4 compliant) and automated testing systems, delivers compliance reports within 72 hours of test completion.
Which environmental tests apply to my product?
Coverage depends on your operating environment and industry: climatic simulation (temperature, humidity, salt spray), dynamic and vibration testing (shock, drop, HALT/HASS), ingress protection (IP ratings), aircraft electrical testing, optical fiber and telecom interface testing, connector testing, and electrical safety testing (e.g., EN 60601-1 for medical devices).
Does my device need cybersecurity testing if it is not internet connected?
The FDA “cyber device” definition is broader than internet connected products. If your device includes software and has any digital interface including USB, Bluetooth, Wi-Fi or removable media you should assume FDA cybersecurity requirements apply and request a scoping assessment.
Can testing services be combined into one engagement?
Yes, Because NexorTest delivers design, testing and regulatory consulting from one team, EMC/EMI, environmental, cybersecurity and usability testing can be scoped and scheduled together reducing timeline and coordination overhead compared to using separate vendors for each discipline.
What is a Software Bill of Materials (SBOM) and why does FDA require it?
A Software Bill of Materials (SBOM) is a machine readable inventory of every software component, library and dependency inside a medical device, including version numbers and known vulnerabilities (CVEs). FDA requires SBOMs in CycloneDX or SPDX format as part of cybersecurity premarket submissions so reviewers and, later, hospital IT teams can identify and respond to vulnerabilities across the device lifecycle.
Ready to Test, Certify and Launch Globally?
Tell us your product and target markets our specialists will scope the exact combination of EMC/EMI, environmental, cybersecurity and usability testing your submission requires.