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Ring Testing Technology (Zhongshan)Co., Ltd.

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India BIS Certification

India BIS Certification

BIS certification is ISI certification and certification agency of Indian Standards (The Bureau of Indian Standards), referred to as BIS, specifically responsible for product certification.。

According to The BIS Act, 1986, the Bureau of Indian Standards (BIS) is responsible for product certification and is the only product certification body in India. BIS has five regional bureaux and 19 sub-bureaux. It was formally established in 1987 to replace the Indian Standards Institute, which had been established in 1946.

The regional bureau supervises the corresponding branch. Eight laboratories affiliated with BIS and a number of independent laboratories are responsible for testing samples taken during the product certification process. These laboratories are implemented in accordance with ISO/IEC 17025:1999.

BIS certification mark

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The ISI mark issued by BIS is a sign that the product complies with Indian standards and is also a proof of compliance with product specifications. All BIS certifications are carried out according to Indian standards, and those that are certified use the common ISI mark.

Many manufacturers now export their products to India, and their products in India need to apply for BIS certification. For applicants, the Mandatory Registration Act mainly emphasizes the following content, registration applicants should pay attention to:

 1. Implementation date.

For locally manufactured products from the date of production, for imported products from the date of import.

For products arriving in India after the effective date, mandatory registration requirements and self-declaration must be followed.

If you enter India after this date, you will not be able to clear customs without a self-declaration label.

2. Registration applicants.

The applicant/holder of the certificate of Registration can be a domestic manufacturer or factory, but the application for registration must be made by its local branch in India or authorized local agent in India to submit the application to BIS until the registration is completed.

3. Product registration code.

The product registration code should be requested by the manufacturer or importer, and the registration code is provided by BIS.

The registration code is associated with the manufacturer, the factory address (even if the factory is overseas), and the product.

Each manufacturing unit needs to be registered independently, even if the same product is produced by the same factory at different sites.

The local authorised representative of the manufacturer (factory) may apply for registration on behalf of the factory.

 4. Test report.

If the product is produced by OEM, and the product has been tested in an overseas laboratory or CB laboratory in accordance with international safety standards or affixed with CE, UL, FCC marks, it also needs to be re-tested.

The e decree requires submission of a valid test report from a BIS accredited laboratory (within 90 days) for mandatory registration.

 5. Self-declaration label.

The label shall be affixed in the format of "' Self-declaration - Compliance with IS** Standard Requirements' Registration number **", and the standard number shall be followed by the year in which the standard was issued separated by ":".

Such as "Self - Declaration - Conforming to IS: 13252 2010" Registration No. * *. * * (" ego statement -- meet IS 13252:2010 "Registration number * *. * *).

Self-declaration should be prioritized on the product. If the size limit cannot be indicated on the product, the declaration may also be indicated on the packaging.

 There is no specific location for Posting the declaration. In accordance with the relevant product safety requirements, the declaration shall be indelible and clearly identified/displayed on the product

 6. The test laboratory

The manufacturer's own laboratory cannot apply to become a BIS accredited laboratory.

At present, only seven Indian laboratories are accredited by the BIS, and the BIS regulates testing fees for various products.

 7. Quality assurance mechanism。

The law does not require testing of every batch.

If the relevant product standard requires this, it is necessary to test each shipment.

Ensuring that products continue to comply with the relevant standards is a requirement of the quality assurance mechanism of the enterprise and is therefore the responsibility of the manufacturer.

 8. Product sampling and testing

If the product has different sizes, classifications or varieties, the test can be based on the series of products.

The registration process is:

①Sample extraction of registered manufacturers will be extracted from manufacturers or markets by regulatory authorities;

②During the registration period, samples of products or series of products should be taken at least once every two years;

③Within the scope of registration, at least one sample of each series of products is taken for testing;

④In addition to the samples to be tested, a sample should also be taken from the batch for use in case of disputes.

 9. Validity of registration

There is no requirement for duplicate registration of the same product and registration is valid for two years once approved.

After the expiration date, the registered entity will need to re-submit samples for testing and re-registration. When the IS standard on which a product is tested is withdrawn, the registration based on that standard is subsequently cancelled.

Manufacturers should stop the supply of old products some time in advance, register them based on the new standard, and change the label on the device.

 10. Model division。

BIS has formulated a specific series of model division criteria for each type of product, and only the same series of models that meet the conditions can be placed in a registration certificate.

At the same time, the decree stipulates that each certificate cannot exceed 10 models, and those that exceed 10 still need to be issued separately.

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