Grounded ESD provides third-party ESD program verification, diagnostics, and documentation for manufacturers operating in regulated and high-reliability environments.
Our services are designed to help you:
We go beyond checklist audits by using diagnostic tools and real-world measurements to show how your ESD controls are actually performing on the floor.
Independent, on-site evaluations of your ESD control program, including:
You receive clear, defensible documentation suitable for customers, internal quality, and regulatory audits.
Verification of ESD control items and systems per ESD TR53, including:
Testing is performed using calibrated, industry-recognized instrumentation.
For facilities experiencing unexplained failures or intermittent issues:
This service helps uncover risks that traditional compliance checks miss.
Verification of ionizer and environmental controls, including:
For companies needing continued confidence and stability:
End-to-end support for building or upgrading Electrostatic Protected Areas.
Grounded ESD develops and updates formal ESD Control Program Plans required for ANSI/ESD S20.20 compliance, customer audits, and regulated manufacturing environments.
This service is ideal for companies that:
What's Included
Why This Matters
A written ESD Control Program is not optional in regulated or high-reliability environments. It is the foundation document that customers and auditors use to judge your program.
We do not provide templates - we build plans that reflect how your facility actually operates, so your documentation is defensible, usable, and audit-ready.
This service is designed for environments where audit defensibility, traceability, and risk prevention are mandatory, not optional.
What's Included
Why This Matters in Defense & Aerospace
We help you move from basic compliance to defensible, stable ESD control that protects mission-critical products and programs.
Typical Environments
Grounded ESD provides specialized ESD verification and stabilization services for medical device manufacturers and cleanroom production environments, where product safety, traceability, and regulatory compliance are critical.
Our services support facilities operating under FDA, ISO 13485, and customer audit requirements, where ESD failures can compromise device reliability and patient safety.
What's Included
Cleanroom-Specific Focus
Why This Matters
in medical manufacturing, ESD failures may not be immediately visible, but they can lead to latent defects, field failures, and regulatory findings.
We help you move beyond basic compliance to defensible, stable ESD control that protects both your products and your quality system.
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