ISO 21702:2019; Anti Viral Claim Verification Testing


Virology Laboratory

ISO 21702:2019 Antiviral Claim Verification Testing

Independent, accredited testing of antiviral activity on plastics and non-porous surfaces — helping you validate product claims with scientific rigor.

Scope of ISO 21702:2019 Testing

The ISO 21702:2019 standard outlines a test method for evaluating antiviral activity on plastics and non-porous surfaces. It is widely used to assess the effectiveness of antiviral coatings and materials, making it critical for industries producing safer, cleaner products for environments where surface contamination is a concern.

Technicians preparing a microbial exposure rig inside a controlled environmental test chamber for ISO 21702:2019 antiviral testing
Exposure Time
24 hours
Standard contact period

Temperature
25°C
Adjustable per product needs

Turnaround
4–6 Weeks
From sample receipt to report

Accreditation
ISO 17025 & GLP
Third-party validation

Materials We Can Test

A broad range of plastics and non-porous surfaces can be tested under this standard:

Plastics and polymers
Coating materials and laminates
Ceramics
Natural and synthetic leathers
Rubbers
Other non-porous surfaces

Test Description

The ISO 21702:2019 test provides a quantitative analysis of the antiviral properties of the surface being tested. The method measures antiviral activity by exposing the test material to viruses under controlled conditions.

The standard typically uses Influenza A virus (H3N2) or Feline Calicivirus as test organisms. We can also adapt the protocol to test against other biosafety level 2 viruses or bacteriophages as per client requirements.

Third-Party Validation

When your product passes ISO 21702:2019 testing at Airmid Health Labs, you receive independent third-party validation of its antiviral activity. This allows you to label your product as tested to ISO 21702:2019 standards, supporting any claims related to antiviral performance.

Why Choose ISO 21702:2019 Testing?

With growing consumer awareness and demand for safer, cleaner surfaces in homes, offices, and public spaces, verifying antiviral activity is more important than ever. ISO 21702:2019 certification is a valuable tool for differentiating your product in competitive markets and demonstrating your commitment to health and safety.

Why Choose Airmid Health Labs

Airmid Health Labs is a world-leading laboratory specializing in indoor air quality and surface testing. Here’s why leading manufacturers trust us with their antiviral testing needs:

ISO 21702:2019 antiviral claim verification testing conducted in a 285 cubic metre environmental test chamber within a GLP and ISO 17025 accredited facility
01

Expertise in Surface Testing

Decades of experience scientifically evaluating the impact of surfaces and materials on health, especially regarding viral and microbial contamination.

02

Customizable Protocols

Flexible testing protocols tailored to your specific product requirements, ensuring antiviral performance is evaluated under the most accurate conditions.

03

State-of-the-Art Facilities

Advanced testing facilities equipped with the latest technology to deliver precise, reliable antiviral testing that meets and exceeds international standards.

04

Independent Credibility

As an ISO-accredited laboratory, our results provide the independent validation your product needs to build consumer trust and meet regulatory requirements.

05

Dedicated Client Support

From initial consultation to delivery of results, our team provides expert guidance throughout the process — ensuring you receive actionable data.

06

Global Industry Trust

Trusted by manufacturers worldwide across consumer goods, medical devices, building products, and transportation sectors.

Ready to Validate Your Antiviral Claims?

Partner with a lab that prioritizes accuracy, scientific integrity, and client satisfaction. Let’s discuss how ISO 21702:2019 testing can strengthen your product claims.

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