Compatible Electronics provides comprehensive IEC 61326 EMC testing for measurement, control, and laboratory equipment. Our NVLAP accredited laboratory holds direct accreditation for IEC 61326-1 and the IEC 61326-2 particular requirements series — covering both emissions and immunity at three California locations.
IEC 61326 specifies EMC requirements for electrical equipment used in measurement, control, and laboratory applications. Unlike generic EMC standards, IEC 61326 addresses the unique challenge these instruments face: they must operate accurately in electromagnetic environments while not generating interference that disrupts nearby equipment.
The standard applies to professional, industrial process, and educational use equipment powered from AC mains, DC supply, or batteries when connected to mains for charging. It covers both emissions (how much interference the equipment generates) and immunity (how well the equipment withstands interference from its environment), with performance criteria tied directly to the equipment's measurement function.
IEC 61326 is the required EMC standard for CE marking under the EMC Directive 2014/30/EU for instrumentation and measurement equipment. EN 61326-1 (the European adoption) is a harmonized standard under this directive, providing presumption of conformity when testing is completed to its requirements.
Compatible Electronics holds NVLAP accreditation for the following IEC 61326 standards, confirmed in our accredited scope effective 2025-06-05 through 2026-06-30:
IEC 61326 requires that the equipment's ability to perform its intended measurement function be assessed during and after each immunity test. The standard defines three performance criteria:
The equipment continues to operate as intended during and after the immunity test. No degradation of performance or loss of function beyond limits specified by the manufacturer.
The equipment may experience temporary degradation of performance during the test, but recovers automatically without operator intervention after the test stimulus is removed.
The equipment may experience temporary loss of function that requires operator intervention (such as a restart) to restore normal operation. Loss of stored data is not permitted unless explicitly allowed.
The acceptable performance criterion for each test is defined by the equipment manufacturer based on the equipment's intended function. IEC 61326-1 specifies default criteria for each immunity test; IEC 61326-2 particular requirements may modify these for specific equipment types.
A manufacturer of a handheld power quality analyzer used in LV distribution systems needed CE marking under the EMC Directive. The instrument is classified under IEC 61326-2-2 (portable test and measuring equipment used in low-voltage distribution systems). Compatible Electronics performed CISPR 11 conducted and radiated emissions (Class B), and the full IEC 61000-4 series immunity test plan with Criterion A performance assessment during signal port and power port tests. The NVLAP accredited EN 61326-1 (2013) test report supported the EU Declaration of Conformity. The same emissions data also supported ICES-003 compliance for the Canadian market.
A process automation manufacturer needed EMC compliance for a modular PLC system deployed in heavy industrial environments. The system was tested to IEC 61326-1 (2013) at the industrial electromagnetic environment test levels — 10 V/m radiated RF immunity, 10 Vrms conducted RF immunity, 2 kV surge on power ports, and 100 A/m magnetic field. Compatible Electronics documented performance criterion A throughout all immunity tests, with the PLC continuing to execute its control program without deviation. The test package supported CE marking under both the EMC Directive and Machinery Directive for the EU industrial market.
A clinical laboratory equipment manufacturer needed dual compliance for an automated biochemistry analyzer: IEC 61326-2-6 for EMC (the IVD-specific part of 61326) and IEC 60601-1-2 Ed. 4 for medical electrical equipment EMC. Compatible Electronics coordinated a combined test plan covering CISPR 11 emissions, the IEC 61000-4 series immunity tests at IVD-appropriate levels, and the additional immunity tests required by IEC 60601-1-2 Ed. 4 for professional healthcare facilities. Performance criterion was assessed against the analyzer's reportable measurement range throughout all immunity tests. The ILAC MRA accredited test reports supported simultaneous CE marking and FDA 510(k) submissions.
NVLAP accredited for IEC 61326-1, -2-1, -2-2, -2-3, and -2-6 at three California locations — not just generic EMC standards.
Complete IEC 61326 package from a single lab — CISPR 11 emissions and the full IEC 61000-4 immunity series in one engagement.
Test reports accepted by EU market surveillance authorities — supporting CE marking Declaration of Conformity without overseas testing.
Experience assessing and documenting Criterion A, B, and C performance during immunity tests for complex measurement and control equipment.
IEC 61326 + IEC 60601-1-2 (medical), IEC 61326 + FCC Part 15, and multi-market packages in a single test session.
Lake Forest/Silverado, Brea, and Newbury Park — all accredited for IEC 61326. Fast turnaround options available.
Contact us for IEC 61326 EMC testing for your measurement, control, or laboratory equipment.
Brea: 714‑579‑0500 · Newbury Park: 805‑480‑4044
www.celectronics.com