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Custom-engineered labels · Since 1978

The right label. A better way to get there.

Engineered labeling solutions for applications where performance matters.

Because what your labels are attached to matters, we help you get the labeling right, make qualification easier, and maintain dependable supply.

CleanMark cleanroom technician adjusting label production equipment in a controlled environment
U.S. engineering & manufacturingISO 9001:2015 certifiedIn-house ISO Class 5 cleanroom
Application results

What getting it right changes.

The difference often shows up in fewer workarounds, simpler handling, and identification that continues to perform.

01 / CLEANROOM · IPA EXPOSURE

No extra cleaning workaround.

A revised direct-thermal label construction stayed readable through heavy IPA cleaning, allowing the intended process to continue without the added label workaround.

Read the cleanroom case study

02 / STERILIZATION · AUTOCLAVE

One label. Fewer handling steps.

An integrated indicator and identification construction removed separate indicator-tape application and removal, while keeping media identity connected to the container.

Read the autoclave case study

03 / DURABLE · DRY ICE

Identification that stays attached.

An engineered adhesive construction addressed labels separating during overseas dry-ice shipping and subsequent handling.

Read the cold-chain case study

A customer’s experience

“They fulfilled on their promise to decrease my delivery time while improving print quality.”

Ernie Schrepfer · Associate Director of Quality, Access Biologicals

Read the customer case study

WHY PERFORMANCE MATTERS

Because what your labels are attached to matters.

Your labels are part of something bigger. From critical manufacturing processes to products people depend on, their performance helps protect the work they support. That’s why we take the time to understand what your labels need to do—and the consequences when they don’t.

SEMICONDUCTOR MANUFACTURING

Material identity through controlled handling.

Traceability and clean removal matter when wafers, carriers, and materials move through precision manufacturing processes.

Explore wafer-box labels

PHARMACEUTICAL MANUFACTURING

Less handling around critical processes.

Integrating identification and process exposure indication can help remove unnecessary steps while maintaining container identity.

Explore sterile labels →

CELL & GENE THERAPY

Identification throughout the cold journey.

Labels may need to withstand disinfectant exposure, cryogenic storage, and retrieval while information remains readable.

Explore cryogenic requirements

THE QUALIFICATION EXPERIENCE

We make getting the right label easier.

When a process changes or a new label is needed, qualification becomes one more project for teams already managing many priorities. We help keep the work organized, decisions clear, and next steps moving—without adding unnecessary effort to your team.

CleanMark technical team reviewing a label construction and application requirements at a whiteboard
01

Get everyone aligned.

Bring quality, engineering, manufacturing, and procurement requirements into one clear starting point.

02

Keep evaluation moving.

Agree on samples, evaluation criteria, responsibilities, and next steps so the project does not stall between handoffs.

03

Make the handoff straightforward.

Carry decisions and approved requirements forward so your team does not have to start over after qualification.

APPLICATION ENGINEERING & EVALUATION

The work that goes into getting it right.

Getting the construction right takes more than choosing a catalog material. Our team combines material selection, application engineering, prototyping, and hands-on testing to develop a solution for your process.

The result is a practical construction to evaluate, supported by the technical work behind it.

01

Select the right materials.

We evaluate facestocks, adhesives, liners, and print methods against your application’s surfaces, exposures, and handling requirements to identify suitable constructions.

02

Prototype and test.

We develop application-specific samples and test critical material properties to help establish performance before you qualify the solution in your process.

03

Engineer for production.

We use evaluation findings to refine the construction, finalize specifications, and establish a repeatable manufacturing process for the approved solution.

OUR SUPPLY STANDARD

On time. In full. In spec.

Once a label is qualified, it needs to keep performing. We carry the approved requirements into manufacturing and ongoing supply, so your team can depend on the labels it has worked to qualify.

01 / ON TIME

Ready when your process is ready.

A delivery date matters because of the production, validation, or shipment planned around it.

02 / IN FULL

The quantity your plan requires.

The complete quantity and format help keep a planned run from being left unfinished.

03 / IN SPEC

The construction you approved.

Materials, print, dimensions, packaging, and applicable requirements need to match the approved specification.

CleanMark manufacturing floor with label converting and printing equipment in operation
Your label application

Tell us what you need your labels to do.

Tell us what the label needs to survive, how it will be printed or applied, and what your timeline looks like. We’ll help identify a clear next step.