How We Work

How We Work

E-Beam Sterilization: A simple 2-step process

Step 1 — Dose Mapping & Qualification

We assess your product and requirements. If appropriate, we test-irradiate your product and evaluate results to develop a custom process for each SKU.

Step 2 — Routine Processing

Once qualified, we can quote processing services according to your volume and commercial requirements.

Step 1

 

Qualifying your product for E-Beam processing

 

Untitled design

What is Dose Mapping and Qualification? 

For E-Beam processing, Dose Mapping and Qualification is the crucial process of determining the optimal electron beam dosage and process parameters for a specific product, ensuring that the radiation dose required for successful sterilization can be delivered within specification and at maximum efficiency. At NextBeam, we also include a processing optimization study whenever possible.

1

Typically completed within 5 days from receipt of the product

Dose_Mapping

All NextBeam qualifications include both dose mapping (per ISO 11137 standard) as well as process optimization when possible

3

We only recommend customers undertake qualification when 90%+ confident in successful completion

2

Comprehensive reports are provided to confirm your product’s preparedness for volume processing

Analysis

We analyze sterility requirements and primary data to assess product suitability for E-Beam. If suitable, we request a sample.

Preparation

Each sample undergoes meticulous preparation. We place dosimeters to measure dose distribution within the product.

Dosing & Data Analysis

We irradiate at least three samples. Our lab extracts data from dosimeters and creates a statistical summary of dose distribution.

Reporting

We generate a comprehensive report summarizing the experiment design and results, confirming process parameters.

Step 2

 

 

Routine E-Beam Processing

 

Untitled design

What is Routine Processing?

Routine Processing refers to the regular or large-scale application of electron beam technology for sterilization or other purposes. Once a product completes the Dose Mapping & Qualification process, it is ready for routine processing using E-Beam radiation.

1

Processing typically completed in 5 days or less from receipt

Untitled design copy

E-Beam is clean, sustainable technology: an all-electric process with that produces no harmful / radioactive materials

specific_dosing

E-Beam tech delivers doses in seconds and is gentler on product than gamma 

Untitled design

Scrap rate below 0.1% and dropping: Minimal waste; maximum efficiency

Receipt

Once a product qualifies, we’re ready to process it. We receive customer products in quantities ranging from a single pallet to multiple truckloads.

Processing

We irradiate the product using the tailored parameters determined during qualification, ensuring optimal results.

Quality Control (QC)

Our on-site dosimetry lab confirms that the received product is dosed within specification, maintaining high-quality standards.

Shipment

We efficiently prepare and load the processed product for pickup by the customer’s carrier. Comprehensive quality records are provided electronically.

Well-Located & Logistically Convenient

NextBeam is strategically positioned for your convenience, situated within a day’s drive of major cities such as Chicago, Minneapolis, Denver, St. Louis, Kansas City, and more, catering to both large and small businesses.

Subscribe to our newsletter to learn about future expansions.

Let's Connect

Complete this form, or email hello@nextbeam.com, and a sterilization expert will get back to you within one business day.

FAQs

How much volume can you process?
Our process is designed to support a wide range of volumes, from a single pallet to multiple truckloads of product.

What is the maximum product size you can process?
The maximum standard product envelope is 50” x 30” x 48”. If you have larger needs, please contact us for further assistance.

What industries do you serve?
We serve a diverse range of industries, including medical devices, lab animal science, laboratory supply, and more.

Quality Leadership

We Meet or Exceed Global Quality Sterilization Standards

Quality system accredited to ISO 13485:2016, Medical devices – Quality management systems – Requirements for regulatory purposes

Quality system accredited to ISO 9001:2015, Quality management systems

Sterilization working group member (WG02)

E61 Radiation processing committee member

FDA-registered establishment