ISI Mark Certification for Manufacturers in India

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A manufacturing company receives a large purchase order for a product covered under a mandatory Quality Control Order. The factory has completed production planning, raw materials have been purchased and the buyer expects dispatch within 30 days. During the final compliance review, the company discovers that it does not have a valid BIS licence or CM/L number.

This is not a minor documentation gap. The manufacturer may be unable to dispatch the goods, use the ISI Mark or legally sell the product after the applicable Quality Control Order becomes effective. Finished stock may remain blocked, testing may need to be repeated and customer commitments may be delayed by several weeks or months.

ISI Mark Certification

ISI Mark Certification for Manufacturers in India should therefore be planned before commercial production begins. Manufacturers need to identify the correct Indian Standard, confirm whether the product is covered by a Quality Control Order, prepare the factory laboratory and complete testing before using the Standard Mark.

The process is governed primarily by:

  • Bureau of Indian Standards Act, 2016
  • BIS Rules, 2018
  • BIS Conformity Assessment Regulations, 2018
  • Scheme-I of the BIS Conformity Assessment Regulations
  • Product-specific Quality Control Orders
  • Applicable Indian Standards
  • Product Manuals and Scheme of Inspection and Testing

What Is ISI Mark Certification?

ISI Mark Certification is a product conformity licence granted by the Bureau of Indian Standards under Scheme-I. It allows a manufacturer to use the BIS Standard Mark, commonly called the ISI Mark, on products manufactured at an approved factory.

The licence is issued against a specific Indian Standard. It is not a general quality certificate for the entire company or all products manufactured at the facility.

For example, if a manufacturer produces 12 different product models, the licence will cover only those grades, varieties, ratings, sizes or models approved by BIS. Any product outside the approved scope cannot automatically carry the ISI Mark.

The licence is also factory-specific. A company operating 3 factories may need separate BIS licences for each manufacturing location, depending on where the certified product is produced.

An ISI-marked product generally displays:

  • The BIS Standard Mark
  • The applicable Indian Standard number
  • The BIS licence number in CM/L format
  • Product-specific marking information
  • Batch, grade, size or model details, where applicable

When Is ISI Mark Certification Mandatory?

BIS certification is voluntary for many products. However, the Central Government can make certification compulsory by issuing a Quality Control Order.

Once the Quality Control Order becomes effective, covered products cannot normally be manufactured, imported, stored, distributed or sold without conformity to the applicable Indian Standard and a valid BIS licence.

Manufacturers should not rely only on the commercial product name. Applicability may depend on technical specifications such as:

  • Material composition
  • Product dimensions
  • Voltage or power rating
  • Grade or classification
  • Intended application
  • Load capacity
  • Safety characteristics
  • Product construction

A manufacturer should check the applicable Quality Control Order at least 3 to 6 months before the planned production or market launch date.

Before applying, the manufacturer should confirm:

  • Whether the product is covered under a mandatory Quality Control Order
  • The exact Indian Standard applicable to the product
  • The implementation date of the Quality Control Order
  • Whether separate dates apply to micro, small or medium enterprises
  • Whether any exemption applies
  • Whether the correct route is ISI, CRS, FMCS or Scheme-X

Regulatory Overview

Regulation or Requirement Main Requirement Timeline Applicable To Business Risk
BIS Act, 2016 Compliance with compulsory standards Before manufacture or sale Manufacturers and importers Seizure, penalty and prosecution
Scheme-I Factory assessment and product testing Before use of ISI Mark Domestic and eligible foreign manufacturers Application rejection
Quality Control Order Mandatory certification requirement Effective date mentioned in the order Covered product categories Production or sales stoppage
Indian Standard Product specifications and testing Continuous Approved product scope Sample failure
Product Manual Testing, grouping and marking requirements During application and licence operation BIS licensees Non-conformity
Scheme of Inspection and Testing Internal quality control and test frequency Throughout licence validity Factory quality team Suspension
BIS licence renewal Continuation of licence Normally before expiry Existing licensees Licence expiry

BIS certification does not replace other factory approvals. A manufacturing unit may separately require Consent to Establish, Consent to Operate, Factory Licence, Fire NOC or hazardous waste authorization.

Similarly, obtaining environmental approvals does not remove the requirement to obtain BIS certification where the product is covered under a mandatory Quality Control Order.

ISI Mark, CRS, FMCS and Scheme-X

Manufacturers frequently use the terms BIS registration and BIS certification interchangeably. However, BIS operates different conformity assessment routes.

Selecting the wrong route can result in incorrect testing, application rejection and loss of several weeks.

Certification Route Main Purpose Applicable Applicant Factory Inspection Approval Type
ISI Mark or Scheme-I Product certification against Indian Standard Indian manufacturer and eligible foreign manufacturer Normally required BIS licence with CM/L number
CRS or Scheme-II Registration of notified electronic and IT products Manufacturer Based on CRS process BIS registration number
FMCS Certification of foreign manufacturing units Foreign manufacturer Foreign factory inspection BIS licence
Scheme-X Certification of notified machinery and electrical equipment Indian or foreign manufacturer As applicable Scheme-X licence

A domestic trader or importer cannot normally obtain an ISI licence in its own name for a product manufactured at a foreign factory. The actual foreign manufacturing unit generally needs to apply under the Foreign Manufacturers Certification Scheme.

Applicable Indian Standard and Product Scope

The first technical step is identifying the correct Indian Standard.

Products that appear similar in the market may have different standards based on their construction, application, material or performance requirements.

For example, a wrong standard selection can result in:

  • Testing under incorrect parameters
  • Purchase of unsuitable machinery
  • Installation of unnecessary laboratory equipment
  • Rejection of the application
  • Restriction of the approved product scope
  • Repeated product testing

After identifying the standard, the manufacturer must study the Product Manual and Scheme of Inspection and Testing.

The Product Manual normally explains:

  • Product grouping
  • Sampling requirements
  • Testing frequency
  • Raw material requirements
  • Marking rules
  • Scope extension requirements
  • Factory laboratory requirements
  • Subcontracting permissions

If a company manufactures 20 product sizes, BIS may not require testing of all 20 sizes. However, representative samples must be selected according to the grouping guidelines.

Incorrect grouping can result in approval for only a limited product range.

Factory Readiness Before Applying

Manufacturers should not apply merely because production machinery has been installed.

The factory must be able to demonstrate consistent production, quality control and testing capability.

During the factory visit, BIS may verify:

  • Manufacturing process
  • Production machinery
  • Raw material controls
  • Laboratory equipment
  • Calibration certificates
  • Quality control personnel
  • Internal test records
  • Product traceability
  • Storage and marking controls
  • Implementation of the Scheme of Inspection and Testing

The normal factory visit for an Indian manufacturer may be completed in approximately 1 working day. More time may be required for complex products, multiple production lines or large product scopes.

The factory should be ready to conduct an actual production run during inspection.

A factory may face delays when:

  • Machinery is installed but not operational
  • Laboratory equipment is unavailable
  • Calibration certificates have expired
  • Quality control staff are not present
  • Raw material records are incomplete
  • Samples cannot be produced during the visit
  • Test procedures are not understood by the laboratory team

Documents Required for ISI Mark Certification

The exact document list depends on the product, business structure and Indian Standard.

However, most applications require business, factory, technical and product documentation.

Business Documents

Business documents confirm the legal identity of the manufacturing entity.

Common documents include:

  • Certificate of incorporation
  • Partnership deed or proprietorship proof
  • PAN
  • GST registration certificate
  • Udyam Registration, where applicable
  • Authorization letter for the signatory
  • Trademark or brand authorization
  • Factory ownership or lease documents

Factory Documents

Factory documents establish that the applicant controls the declared manufacturing facility.

These may include:

  • Factory layout
  • Location plan
  • Manufacturing process flow
  • List of production machinery
  • Installed production capacity
  • Factory Licence
  • Consent to Establish
  • Consent to Operate
  • Fire NOC
  • Other product-specific approvals

Quality Control Documents

Quality documents demonstrate the factory’s ability to maintain product conformity.

These may include:

  • List of laboratory equipment
  • Calibration certificates
  • Qualification details of quality control staff
  • Internal testing formats
  • Raw material test certificates
  • Quality assurance plan
  • Scheme of Inspection and Testing records
  • Third-party laboratory reports

Product Documents

Product documents establish the requested licence scope.

These may include:

  • Product drawings
  • Technical specifications
  • Product catalogue
  • Model or grade list
  • Applicable Indian Standard
  • Grouping justification
  • Product test report
  • Marking and labelling artwork

Company name, factory address and product description should remain consistent across all documents.

Even a small mismatch in the factory address may lead to a clarification query and delay the application by 7 to 15 working days.

ISI Mark Certification Process for Manufacturers

The BIS application process should begin only after the factory and product are technically ready.

Step 1: Applicability Assessment

The manufacturer should review the product description, Quality Control Order, Indian Standard and implementation date.

The assessment should confirm:

  • Whether certification is mandatory
  • Which BIS scheme applies
  • Whether the applicant is the actual manufacturer
  • Whether any exemption is available
  • Which models or grades need certification

This step may take approximately 2 to 5 working days.

Step 2: Factory Gap Assessment

The factory’s machinery, laboratory and quality system should be compared with the Indian Standard and Product Manual.

The assessment should identify:

  • Missing laboratory equipment
  • Calibration requirements
  • Testing gaps
  • Raw material compliance gaps
  • Documentation weaknesses
  • Manpower requirements

Depending on factory readiness, corrective action may take 1 to 4 weeks.

Step 3: Product Testing

A representative product sample is prepared according to grouping guidelines.

The sample may be tested in a BIS-recognised or accepted laboratory, depending on the application route.

Testing time may vary from:

  • 3 to 7 days for basic physical tests
  • 10 to 30 days for detailed mechanical or electrical tests
  • More than 30 days for long-duration performance tests

Step 4: Online Application

The manufacturer submits the application through the BIS online system.

The application generally includes:

  • Company information
  • Factory details
  • Indian Standard
  • Product scope
  • Test report
  • Manufacturing process
  • Quality control information
  • Government fee payment

Step 5: Application Scrutiny

BIS reviews the documents and may raise queries.

Common queries relate to:

  • Product scope
  • Test report validity
  • Factory address
  • Grouping
  • Laboratory facilities
  • Calibration certificates
  • Raw material conformity

A manufacturer should respond to queries within the portal timeline to avoid closure or rejection.

Step 6: Factory Inspection

The BIS officer visits the manufacturing facility.

The inspection may include:

  • Verification of production machinery
  • Demonstration of manufacturing process
  • Laboratory inspection
  • Review of test records
  • Verification of calibration
  • Sample drawal
  • Verification of quality personnel
  • Review of marking arrangements

Step 7: Grant of Licence

If the factory assessment and product test results are satisfactory, BIS grants the licence.

The licence includes:

  • CM/L number
  • Applicable Indian Standard
  • Approved product scope
  • Licence validity
  • Marking fee conditions
  • Scheme of Inspection and Testing

Option 1 and Option 2 Processing

BIS provides different application processing routes under Scheme-I.

The applicable route depends on the product, applicant category and BIS instructions.

Option 1

Under Option 1, BIS conducts the factory assessment and arranges sample drawal for independent testing.

Foreign manufacturers generally proceed under Option 1.

The official target for completing an eligible Option 1 application may be up to 90 days from the date of receiving a complete application.

The 90-day period is conditional. It may increase if:

  • Documents are incomplete
  • Factory inspection is unsatisfactory
  • Product testing is delayed
  • Samples fail
  • The applicant does not respond to queries
  • Additional testing is required

Option 2

Option 2 is available for eligible domestic manufacturers and eligible products.

Under this route, the manufacturer normally submits acceptable test reports before the factory visit.

The target processing period may be approximately 30 days from receipt of the complete application, provided the factory visit and product conformity are satisfactory at the first instance.

For an all-India first product case, the processing target may extend to approximately 45 days.

The latest test report should generally not be more than 90 days old when submitted. Where multiple reports are used, the oldest supporting report may need to remain within approximately 180 days.

Manufacturers should not assume that Option 2 is available for every product.

Compliance Timeline

The following timeline is a practical planning estimate. Actual approval depends on product complexity, testing duration and factory readiness.

Step Responsible Authority Approximate Timeline Main Requirement Risk
Product and standard mapping Manufacturer 2-5 working days QCO and Indian Standard review Wrong certification route
Factory gap assessment Manufacturer 5-15 working days Machinery and laboratory review Inspection failure
Calibration and corrective action Factory 1-4 weeks Valid calibration and equipment Application delay
Product testing Laboratory 7-30 days Representative sample Sample failure
Online application Manufacturer 1-3 working days Complete technical file Portal query
BIS scrutiny BIS 5-15 working days Document verification Clarification delay
Factory inspection BIS Normally 1 working day Production and testing demonstration Repeat visit
Option 2 processing BIS Approximately 30 days First-instance conformity Suspension after failed sample
Option 1 processing BIS Up to approximately 90 days Inspection and test conformity Long testing period
Licence renewal BIS Before expiry Production and fee records Expiry of licence

Manufacturers should ideally begin preparation at least 90 to 120 days before a mandatory Quality Control Order becomes effective.

Product Testing Requirements

Testing is one of the most important parts of ISI certification.

The product must conform to all mandatory clauses of the applicable Indian Standard.

The manufacturer should confirm that:

  • The laboratory is authorised for the applicable standard
  • All required test clauses are covered
  • The test report matches the proposed product model
  • The report is within the permitted validity period
  • The sample represents the proposed licence scope
  • Long-duration tests are identified in advance
  • Raw material test reports are available where required

Testing does not end after licence grant.

The manufacturer must continue conducting internal tests according to the Scheme of Inspection and Testing.

The required frequency may be:

  • Every batch
  • Every shift
  • Daily
  • Weekly
  • Monthly
  • Once in 3 months
  • Once in 6 months

The actual frequency depends on the product and test requirement.

ISI Certification Cost

There is no single fixed cost for all ISI Mark applications.

The total cost depends on:

  • Product type
  • Indian Standard
  • Number of product varieties
  • Number of samples
  • Laboratory testing charges
  • Inspection duration
  • Factory location
  • Marking fee
  • Scope extension requirements
Cost Component Cost Basis
Application fee BIS processing charge
Factory inspection fee Number of inspection days
Product testing fee Test parameters and laboratory
Annual licence fee Generally around ₹1,000
Minimum marking fee Product-specific
Actual marking fee Based on certified production
Renewal fee Licence period and production
Scope extension fee Additional models or varieties
Professional support fee Documentation and technical preparation

Testing charges may range from a few thousand rupees to more than ₹1 lakh, depending on product complexity.

The minimum marking fee is product-specific and may remain payable even when actual production is lower than the declared quantity.

Manufacturers should prepare a separate budget for:

  • Laboratory equipment
  • Calibration
  • Sample preparation
  • Product testing
  • BIS fees
  • Factory modifications
  • Quality control manpower

Validity and Renewal

An initial ISI licence may generally be granted for a period between 1 and 2 years.

After the initial period, the licence may be renewed for a period of up to 5 years, subject to satisfactory performance and payment of applicable fees.

The renewal application should normally be submitted at least 2 months before the licence expiry date.

For example, if the licence expires on 31 December, the renewal process should ideally begin before 31 October.

The manufacturer should maintain a renewal calendar covering:

  • Licence expiry
  • Calibration expiry
  • Internal testing schedules
  • Production statements
  • Marking fee calculations
  • Surveillance observations
  • Indian Standard amendments
  • Product scope changes

Failure to renew the licence on time may interrupt production and prevent continued use of the ISI Mark.

Rules for Using the ISI Mark

The ISI Mark can be used only after BIS grants the licence.

The manufacturer cannot print or use the ISI Mark during the application stage.

The mark can only be used on products included in the approved licence scope.

Manufacturers must not:

  • Print the ISI Mark before approval
  • Use another manufacturer’s CM/L number
  • Mark an unapproved model
  • Continue marking after licence expiry
  • Continue marking during suspension
  • Transfer the licence to another factory
  • Use the mark on failed products
  • Hide changes in production location

The marking should normally include:

  • Standard Mark
  • CM/L number
  • Indian Standard number
  • Product grade or model
  • Batch or manufacturing details
  • Other mandatory information

Compliance Risks and Penalties

Application Rejection

An application may be rejected if the factory does not have adequate production or testing capability.

Rejection may also occur when:

  • Product conformity is not established
  • Documents remain incomplete
  • Factory inspection is unsatisfactory
  • Test reports are invalid
  • The applicant does not respond to BIS queries

A rejected applicant may need to correct the deficiencies and submit a fresh application.

Licence Suspension

A licence may be suspended when:

  • Surveillance samples fail
  • Internal testing is not conducted
  • The manufacturer violates marking requirements
  • Production is shifted without approval
  • The manufacturer produces non-conforming goods
  • Inspection access is denied

Under certain Option 2 cases, failure of the verification sample may lead to immediate suspension.

The manufacturer may be required to implement corrective action and submit a fresh sample within approximately 30 days.

Product Recall and Stop-Sale Direction

BIS may direct a manufacturer to stop supplying and selling non-conforming products carrying the Standard Mark.

The manufacturer may also be required to recall products already supplied in the market.

This can result in:

  • Dealer returns
  • Customer claims
  • Transport costs
  • Repacking expenses
  • Production stoppage
  • Brand damage

Financial and Criminal Penalties

Unauthorised manufacture or sale of compulsory products may attract imprisonment of up to 2 years.

The financial penalty may include:

  • Minimum ₹2 lakh for the first contravention
  • Minimum ₹5 lakh for a second or subsequent contravention
  • Fine extending up to 10 times the value of the goods involved

Company directors, managers and responsible officers may also face liability where the violation occurred with their consent, knowledge or negligence.

Case Study: Manufacturing Without a Valid ISI Licence

A welding electrode manufacturer continued manufacturing and storing a product covered under a mandatory Quality Control Order without holding the required BIS licence.

During enforcement action, authorities reportedly found more than 250 boxes of finished products and over 50,000 units of packaging material.

The estimated value of the material was approximately ₹10 lakh.

The company faced risk not only because finished products were available, but also because packaging material was prepared for products requiring mandatory certification.

This case study highlights 4 important compliance lessons:

  • Quality Control Order applicability should be checked before production
  • ISI packaging should not be printed before licence grant
  • Finished stock should not be manufactured for commercial sale without approval
  • Product, packaging and production records can all be examined during enforcement

Common Reasons for Delay

Most delays are caused by technical gaps rather than the online application form.

A manufacturer may have complete company documents but still fail because the factory cannot perform a mandatory test.

Another company may have adequate machinery but submit a sample that does not represent the full product range.

Common delay factors include:

  • Wrong Indian Standard
  • Incorrect product grouping
  • Expired calibration certificate
  • Incomplete test report
  • Missing laboratory equipment
  • Unqualified quality control personnel
  • Address mismatch
  • Lack of production during inspection
  • Incomplete raw material records
  • Delayed response to queries
  • Incorrect marking artwork

A technical pre-assessment can reduce the risk of repeated testing and repeat inspection.

Practical Compliance Planning

Manufacturers should work backwards from the expected market launch date.

If a Quality Control Order becomes effective on 1 October, the company should not wait until September to begin testing.

A safer preparation plan may look like this:

  • Month 1 – Product and standard assessment
  • Month 1 – Factory gap review
  • Month 2 – Laboratory setup and calibration
  • Month 2 – Trial production and sample testing
  • Month 3 – BIS application
  • Month 3 or 4 – Factory inspection
  • Month 4 – Licence grant, subject to conformity

The company should assign responsibilities to:

  • Production team
  • Quality control team
  • Purchase team
  • Compliance team
  • Finance team
  • Management representative

Certification becomes difficult when the entire process is handled by an external consultant without factory participation.

Conclusion

ISI Mark Certification for Manufacturers in India is not limited to obtaining a certificate.

It is a continuing system covering product design, raw material control, production, testing, marking, inspection and renewal.

Manufacturers should identify the correct Indian Standard, prepare the factory laboratory, complete representative testing and maintain product conformity throughout the licence period.

The cost of early preparation is usually lower than the risk of rejected stock, repeat testing, delayed orders, licence suspension or enforcement action.

A delay of 30 to 90 days can affect production schedules, customer contracts and working capital. A penalty can begin from ₹2 lakh and may extend up to 10 times the value of the affected goods.

Early compliance planning helps manufacturers protect market access, maintain production continuity and reduce the possibility of rejection.

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Frequently Asked Questions

Manufacturers of products covered under a mandatory Quality Control Order must obtain the applicable BIS licence before manufacturing or selling the product.

Eligible Option 2 applications may be completed in approximately 30 days. Option 1 applications may take up to approximately 90 days, provided the application, inspection and testing are satisfactory.

Factory inspection is normally required under Scheme-I. BIS verifies production machinery, laboratory equipment, quality personnel, calibration and manufacturing controls.

The initial licence may generally be valid for 1 to 2 years. Renewal may be granted for a further period of up to 5 years.

An Indian importer cannot normally obtain the manufacturing licence in its own name for a foreign-produced product. The foreign manufacturer generally applies under FMCS.