Testing and verification
Project-based TID, bias, monitoring, data review and reporting from initial protocol to controlled deliverables.
中文Request a testABOUT ACCURAD
Semiconductor radiation effects, made actionable
AccuRad® supports semiconductor R&D, reliability and engineering teams with test planning, controlled execution, data interpretation and reportable outcomes.
WHAT WE DO
Connect test conditions, device response and engineering decisions
Contract testing is the primary route. Device studies, data interpretation, TID systems and laboratory implementation extend the same specialist platform.
Device and application programs
Verification paths for power devices, digital ICs, memory, sensors and electronic modules, defined around application risk.
Systems and laboratories
TID-X systems, dosimetry, fixtures, instrumentation, software, methods and implementation support for internal capability.
WORKING PRINCIPLES
Clear conditions. Traceable data. Actionable outcomes.
A useful result explains how it was produced, where it applies and what the engineering team can do next.
Question-led
Define the device, application and risk question before dose, bias, checkpoints and deliverables.
Condition-traceable
Key configurations, measurement points, data sources and deviations remain available for review.
Boundary-explicit
Observed data, engineering interpretation and hypotheses are presented at the appropriate evidence level.
Information-conscious
Public channels accept only non-sensitive outlines; protected information follows an agreed handoff.
PROJECT EXPERIENCE
From an initial question to a controlled deliverable
Each phase has a clear input, output and communication point, so the customer can see what has been agreed and what happens next.
Question and scope
Clarify the device, application, test variables, samples, schedule and expected output.
Test and record
Execute the agreed plan and record dose, bias, checkpoints, exceptions and relevant deviations.
Data and protection
Use project information within the agreed scope and transfer protected material through an agreed method.
Outcome and next step
Deliver data, reporting and applicability boundaries, then discuss retest or engineering follow-up.
PROJECT INTAKE
Start with the engineering question
Share a non-sensitive device category, test objective, target dose, bias conditions and schedule. We will route the request to the appropriate specialist.