Independent consultancy — not affiliated with AERB
AERB & Radiation Safety Compliance
End-to-end AERB, eLORA, regulatory documentation and radiation-safety support for manufacturers, suppliers and end users of X-ray and scanning equipment in India.
Independent consultancy • Practical industry experience • Documentation-focused support
Technical overview
India · B2BEngineering-style overview only — not an AERB certificate or government endorsement.
Practical industry experience
Hands-on experience with AERB and eLORA workflows, regulatory documentation, AERB queries and radiation-safety compliance activities for X-ray and scanning equipment.
AERB compliance lifecycle
A practical engineering-style view of common stages. Exact pathway depends on equipment category and current requirements.
Institution / Supplier Readiness
NOC
Type Approval
Equipment Registration
eLORA / Compliance
Renewal / Ongoing Compliance
Institution / Supplier Readiness
NOC
Type Approval
Equipment Registration
eLORA / Compliance
Renewal / Ongoing Compliance
Who we help
Choose the path that matches your role in the equipment lifecycle.
From institution/supplier readiness to Type Approval, model additions, renewals and documentation discipline for manufacturing teams.
Typical requirements
Practical support for Indian suppliers and distributors handling imported X-ray/scanning lines and recurring regulatory activity.
Typical requirements
Help for institutes and facilities that need clear end-user registration and procurement-permission support without regulatory overclaim.
Typical requirements
Start here
Select the scenario closest to your current requirement.
Type Approval / NOC / Documentation
Continue 2NOC / OEM documentation / regulatory pathway
Continue 3Query analysis / response support
Continue 4Gap analysis / corrective documentation
Continue 5Renewal / amendment / ongoing compliance
Continue 6Registration / procurement permission / safety compliance
ContinueCore services
Consultancy support for documentation, process coordination and practical radiation-safety activities within applicable qualifications.
Institution registration, supplier authorization, NOC, Type Approval, equipment registration, renewals and amendments.
Application preparation, submission support, tracking, query handling and non-compliance assistance on eLORA.
Documentation, survey support, leakage-check coordination and safety programme assistance within applicable qualifications.
Checklists, gap analysis, technical dossiers, OEM reviews and pre-submission audits.
Monthly retainers, annual compliance management and new-model regulatory support.
Imported OEM support
Practical support for Indian suppliers bringing applicable X-ray/scanning equipment into India — focused on OEM documentation, NOC and Type Approval readiness.
Understand the observation. Identify the gap. Prepare the response.
Support with understanding observations, identifying documentation gaps and preparing/coordinating appropriate responses. No approval outcome is guaranteed.
Equipment coverage
Applicable requirements are assessed case by case against current regulatory requirements.
Security screening systems used in airports, buildings and logistics environments.
Regulatory support may include pathway assessment, documentation review and process coordination.
Mobile inspection systems requiring careful model and documentation control.
Regulatory support may include pathway assessment, documentation review and process coordination.
Compact scanning devices where category-specific requirements must be confirmed.
Regulatory support may include pathway assessment, documentation review and process coordination.
Analytical systems commonly appearing in AERB consumer/scanning guidance sets.
Regulatory support may include pathway assessment, documentation review and process coordination.
Cabinet/handheld XRF where applicable under current guidance.
Regulatory support may include pathway assessment, documentation review and process coordination.
XRD systems supported where demonstrated scope and requirements apply.
Regulatory support may include pathway assessment, documentation review and process coordination.
Inspection systems used in food production/quality contexts.
Regulatory support may include pathway assessment, documentation review and process coordination.
Larger scanning systems within demonstrated consultancy scope.
Regulatory support may include pathway assessment, documentation review and process coordination.
Additional applicable categories assessed case by case against current AERB guidance.
Regulatory support may include pathway assessment, documentation review and process coordination.
Preparation checklist
Consultant profile
Independent regulatory compliance support grounded in manufacturing-side AERB/eLORA experience — focused on documentation quality, process coordination and practical radiation-safety activities within applicable qualifications.
View full profileRupali Pawar
India · Independent consultancy
11+ years in radiation safety and AERB compliance · BE · Former RSO Officer. Independent consultancy — no AERB affiliation is claimed.
Case studies
Client names and approval outcomes are published only with permission. These examples describe support scope, not guaranteed results.
Challenge
An Indian supplier needed structured regulatory support for applicable imported X-ray inspection equipment, including documentation readiness and pathway clarity.
Support
Outcome
Outcome details are published only with client permission. Contact us to discuss anonymized engagement examples relevant to your equipment category.
Challenge
An applicant received regulatory observations and needed practical help identifying documentation gaps and preparing a coherent response pack.
Support
Outcome
No approval outcome is implied. The engagement focused on clarifying observations and coordinating documentation corrections.
Resources
Educational summaries — always verify against current official AERB guidance.
An educational introduction to eLORA for manufacturers, suppliers and end users working with X-ray and scanning equipment compliance in India.
A careful comparison of how NOC and Type Approval are commonly discussed for imported X-ray/scanning equipment, with emphasis on case-specific confirmation.
A plain-language overview of how manufacturers and suppliers typically approach AERB pathways for X-ray inspection systems — without promising outcomes or timelines.
Share your equipment category, origin and current status — we will outline a practical next-step plan.
Enquiry
A short form to start the conversation. Use the Contact page for full equipment and document details.
Prefer the full form? Go to Contact
