AERB Approval

Type Approval

AERB Type Approval, or Type Registration, certifies that a model of radiation-emitting equipment meets the safety specifications of the applicable AERB code. For X-ray based equipment such as X-ray inspection systems, food scanners, X-ray diffractometers and handheld or cabinet XRF devices and PCB analysers, foreign-make suppliers must obtain it through eLORA before sale. Source Type Approval applies to equipment with radioactive sources made in India.

We prepare supplier registration, technical files and test data and file.

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Service Overview

What is Type Approval?

Type approval is AERB’s approval of the design or model of equipment containing radiation sources or X-ray generators, evaluated against the AERB Safety Code and standards. It is granted to the model, after which units of that model can be supplied and licensed. For diagnostic X-ray equipment, models must be AERB type-approved before users can buy them, and X-ray tube and tube-insert models must be registered through eLORA.

Documents include technical documentation of the model, specifications, shielding and safety interlocks, radiation leakage and performance data, test reports, samples or prototype under NOC, evaluation tables for self-shielded equipment and declarations including lifetime servicing for diagnostic X-ray equipment. Fees and validity were not retrieved.

Type Approval

Who Needs This Service

X-ray equipment and tube manufacturers, suppliers and importers, and makers of scanners, XRF and XRD and inspection systems need type approval.

Brands planning new models should plan testing.

Users need approved models.

If you only resell approved models, check supplier authorisation.

Key Benefits

  • Model approved for supply
  • Technical file prepared
  • eLORA filing
  • Test coordination
  • Market access

Next Steps & Related Services

After approval, supply to licensed users. Related services: NOC, Diagnostic X-ray licence and RSO.

Common Mistakes

  • Incomplete technical file.
  • No prototype NOC.
  • Ignoring updates.
  • Selling unapproved models.
  • Weak servicing plan.

Timeline, Costs & Practical Tips

Timelines depend on evaluation.

Practical tip: prepare test data early.

Additional Information

Type approval ensures equipment design meets safety codes.

Practical Scenarios

Scenario 1:

A maker gets approval.

Scenario 2:

An importer approves a model.

Scenario 3:

A supplier registers tubes.

Process & Planning

A type approval plan starts with the model's technical dossier: specifications, shielding, interlocks, radiation leakage and performance data, test reports and a servicing commitment. Register as a supplier on eLORA, import a prototype under NOC if required, submit the application and respond to AERB's evaluation. Once approved, the model appears in eLORA so users can buy it. Planning checklist: freeze the design before testing, retain test evidence, maintain manufacturing consistency and inform AERB of significant design changes.

Written By

Raghav Sharma, Operations Executive

Raghav Sharma

Operations Executive

10+ Years Experience

As seen on

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Raghav Sharma has 10+ years of experience covering Company Registration - Operation, MCA Services - Operation, Corporate Operation, Import Export Services - Operation, Goverment Licence Services - Operation, FSSAI - Operation, SEBI - Operation, Labour Compliance - Operation, Fund Raising - Operation, Licence & Certificate - Operations.

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Frequently asked questions

Need clarity?

Why is type approval needed?

Users can select only type-approved models in eLORA.

Is it per model?

Yes.

What data is needed?

Technical specs, shielding and test data.

Is servicing required?

Lifetime servicing is a declaration for diagnostic X-ray equipment.

Showing 4 of 4 questions.

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