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Product conformity

BIS certification, matched to the product

Find the applicable Indian Standard and route—ISI, CRS, FMCS, Scheme-X or another BIS scheme—before testing or filing.

Professional fee
Written quote
Working timeline
Scheme and authority controlled; confirmed after product screening
Government charges
Shown before payment
Manufacturing quality team reviewing a regulated product

Built for

Indian and foreign manufacturers

Best when

Product, factory and market are defined

01Screen product
02Choose scheme
03Test and prepare
04BIS review
05Mark and maintain
A practical fit check

Which BIS scheme
fits the product?

Product category and manufacturing location decide the route—not the phrase “BIS certificate”.

ISI / Scheme-I

Factory-based product certification for many products covered by Indian Standards and Quality Control Orders.

CRS / Scheme-II

Self-declaration registration supported by recognised-laboratory testing for notified electronics, IT and related goods.

FMCS

Eligible foreign factories use a manufacturer-facing route with an Authorised Indian Representative.

Scheme-X and others

Covered machinery, hallmarking and management systems each follow distinct conformity-assessment frameworks.

BIS Product Certification

Right standard. Right scheme. Right evidence.

There is no universal BIS registration.

A test report, ISI licence, CRS number and FMCS licence are not interchangeable. Product notification, factory location and scheme rules control the path.

01 / Outcome

What you receive,
ready to use.

We first determine whether the product belongs under ISI, CRS, FMCS, Scheme-X, hallmarking or systems certification, then scope testing, factory readiness and the correct application.

INDIAN STANDARD
PRODUCT · FACTORY · SCHEME
BIS APPROVALYour product route,
properly scoped.
ISI · CRS · FMCS
01

Product and Quality Control Order screening

02

Scheme and Indian Standard identification

03

Manufacturer and factory eligibility review

04

Testing and application evidence plan

05

Licence, marking, surveillance and renewal calendar

02 / Eligibility

What must be
in place.

01

A manufacturer—not merely a trader—responsible for the product at the declared manufacturing location.

02

A product covered by the relevant Indian Standard and, where compulsory, the current Quality Control Order.

03

Manufacturing and quality-control capability appropriate to the selected scheme.

04

A test report from the required recognised laboratory where applicable.

05

For eligible foreign factories, an Authorised Indian Representative and India-facing legal undertakings.

06

Certification ordinarily attaches to the manufacturer and a defined factory—not merely a trader, importer or brand owner.

Start with product and factory

The same commercial brand can need different approvals for different products and factories.

DecisionISI / Scheme-ICRS / Scheme-IIFMCS
Common fitIndian factory and covered productNotified electronics, IT or solar productEligible foreign factory
Core evidenceFactory controls, testing and assessmentRecognised-lab report and declarationFactory assessment, AIR and testing
IdentifierStandard Mark / licenceRegistration numberStandard Mark / licence
03 / Process

From product screening to
lawful marking.

The live compulsory list, standard and product grouping are checked before samples enter a laboratory.

01

Product screening

Step 1

We handle

Check product, model, intended use, manufacturing country and live compulsory list.

You provide

Share specifications, photographs, labels, factory location and target market date.

02

Scheme and standard

Step 2

We handle

Identify ISI, CRS, FMCS, Scheme-X or another BIS route and the applicable standard.

You provide

Confirm the manufacturer, brand, model family and authorised Indian representative if needed.

03

Testing and readiness

Scheme dependent

We handle

Map sample testing, factory controls and the scheme-specific document checklist.

You provide

Arrange compliant samples, facilities, records and authorised access.

04

Application and assessment

Authority controlled

We handle

Prepare filing records and coordinate correctable queries, audit or inspection readiness.

You provide

Authenticate, pay official charges and support factory or product verification.

05

Mark and surveillance

After grant

We handle

Check scope, marking rules, renewal and surveillance dates.

You provide

Use the mark only for covered products and maintain production and test records.

04 / Documents

A checklist without
the back-and-forth.

We ask only for records or data relevant to your application, review, or audit scope.

  • Technical specification, model and brand list
  • Applicable Indian Standard or buyer requirement
  • Product labels, manuals and photographs
  • Current Quality Control Order context

Before you begin

Use clear PDF, JPG, or PNG files.

Keep address records recent and readable.

05 / Fees

Transparent fees,
before you commit.

Each registration carries its own government fee, and some are state-specific. We quote the exact combination for your business before any work begins.

Your written quote covers

  • — Product screening
  • — Scheme and standard
  • — Testing and readiness
  • — Application and assessment
  • — Mark and surveillance
Request a written quote

Not included automatically

  • — Product and scheme-specific BIS application, licence or registration fees
  • — Recognised-laboratory testing and sample costs
  • — Factory inspection, auditor travel and overseas assessment costs
  • — Marking fee, bank guarantee, calibration or facility upgrades

Costs that can repeat

  • — Product or factory surveillance
  • — Licence or registration renewal under the selected scheme
  • — Periodic testing and quality-control records
  • — Scope extension for new models, brands, standards or factories
06 / After registration

Approval received,
scope must stay controlled.

Use the mark only for covered products and maintain testing, quality, surveillance and renewal records.

01

Surveillance

Scheme specific

BIS may conduct factory, market or product surveillance during the licence period.

02

Renewal

Before scheme expiry

Validity differs by scheme; use the exact dates and current renewal rules on the approval.

03

Scope extension

Before adding products

New models, brands, standards or factories may require testing and approval before marking.

04

Quality records

Ongoing

Maintain prescribed production, test, calibration, complaint and marking records.

07 / Questions

Got questions?
We’ve got answers.

Get clarity on compulsory certification, ISI, CRS, FMCS, Scheme-X, testing, fees, scope and surveillance.

Still deciding?

AI CA can compare structures around cost, risk, compliance, and funding.