Home / BIS Certification Consultant in India

BIS certification consulting

Understand the right BIS requirement before you apply.

Standix Global helps Indian and international manufacturers, importers and brand owners identify the BIS requirements applicable to their products and follow the appropriate path towards compliance.

A product name does not tell the whole regulatory story.

A product intended for the Indian market may require certification or registration with the Bureau of Indian Standards. The applicable Indian Standard, certification scheme and application route can depend on the product’s function, technical characteristics, manufacturing location and the relevant government notification.

Products with similar commercial descriptions may have different specifications or intended applications. Those differences can affect the standard, product category or certification route that should be considered.

Our initial review helps you understand:

Whether a mandatory BIS requirement appears to apply
Which Indian Standard and product category should be considered
Whether the appropriate route is CRS registration, an ISI Mark licence or FMCS
What testing, documentation and manufacturing information may be required
Which questions need clarification before an application is prepared

This assessment can prevent a project from beginning under an unsuitable category or certification route.

Principal routes

Understanding the principal BIS routes

BIS operates different conformity-assessment schemes. The correct route should be established for the specific product rather than selected only by familiarity with a particular term.

BIS CRS Registration

The Compulsory Registration Scheme applies to notified electronic and information-technology products. Under this route, the product is tested by a BIS-recognised laboratory and the manufacturer applies for registration for the relevant product, brand and manufacturing location.

Standix Global assists with product-category and standard review, documentation preparation, testing coordination and the registration application. Where several models or brands are involved, we also help examine how they should be presented within the applicable requirements.

BIS ISI Mark Certification

Scheme I is the product-certification route associated with the BIS Standard Mark, commonly called the ISI Mark. For products covered by a mandatory Quality Control Order, the manufacturer must hold the applicable BIS licence before applying the mark and placing the covered product on the Indian market.

This route may involve an assessment of the manufacturing facility, its process controls, testing capabilities and the product’s conformity with the relevant Indian Standard.

Standix Global supports manufacturers with the applicable-standard review, application documentation, testing arrangements and preparation for the factory assessment and licensing process.

BIS FMCS Certification

The Foreign Manufacturers Certification Scheme enables eligible manufacturers whose production facilities are outside India to obtain a BIS licence for products covered by the relevant Indian Standards.

FMCS generally applies to products other than electronic and IT products notified under CRS. The foreign manufacturer is the applicant and must nominate an Authorised Indian Representative in accordance with the applicable requirements.

We assist foreign manufacturers with application preparation, AIR-related documentation, testing coordination and factory-inspection readiness, as relevant to the product and application.

How we support you

How Standix Global supports your BIS project

Our support begins before filing. We first establish what appears to apply and identify the information that must be confirmed. Once the scope is clear, our work may include:

Regulatory applicability assessment

We review available product information against the relevant standards, certification schemes and mandatory requirements.

Indian Standard and product-category review

We help establish the standard and product classification that should be evaluated for the proposed application.

Documentation preparation

We organise the required business, manufacturing, technical, brand and authorisation documents and identify missing or inconsistent information.

Testing support and laboratory coordination

Where laboratory testing is required, we help clients coordinate the testing process with BIS-recognised laboratories.

Application support

We prepare and coordinate the agreed application activities, monitor queries and help the applicant respond with the required information.

Factory-assessment preparation

For certification routes involving a manufacturing-site assessment, we help the manufacturer understand the expected documentation, production controls and testing arrangements.

Post-approval support

Where agreed, we assist with matters such as model or brand inclusion, changes in scope, renewals and ongoing compliance activities applicable to the licence or registration.

Practical experience

Regulatory experience grounded in practical execution

Standix Global is supported by a team of regulatory professionals, each bringing more than six years of experience in compliance consulting.

Our team’s experience covers regulatory requirement assessment, certification planning, documentation, testing coordination, application management, regulatory queries, renewals and post-approval support. We have worked with Indian businesses and overseas manufacturers across multiple markets, including Europe, North America and Asia.

This experience helps us look beyond the application itself. We consider how product classification, applicable standards, manufacturing arrangements, regulated components and supporting documentation may affect the complete compliance route.

We examine the complete compliance picture

Regulatory projects can become complicated when attention is given only to the final product. A product may contain components that are independently covered by mandatory requirements, and their compliance status can affect the testing or registration of the main product.

Our team reviews these dependencies at the beginning of the engagement. We explain what needs to be addressed, how the different requirements are connected and what sequence may be appropriate before the client commits to a course of action.

The purpose is to give the client a practical compliance plan—not simply a list of documents.

Practical example

A practical example from BIS CRS projects

A common issue in BIS CRS projects arises when a manufacturer plans registration for a finished product without first considering the compliance status of its regulated components.

For example, lithium cells and the batteries assembled using those cells may require separate BIS registrations. Similarly, a finished product may incorporate covered components whose registration status must be considered as part of the wider project.

Our team has identified these dependencies during the initial review of multiple CRS projects. By explaining them before the work begins, we help clients understand the complete requirement, evaluate the necessary registrations and plan testing in an appropriate sequence.

Where current BIS provisions permit eligible products to use parallel testing, we explain the applicable conditions and help plan the component and finished-product activities accordingly. This can reduce avoidable waiting time, but the route must be checked against the current product-specific requirements before it is recommended.

Our working approach

Clear advice, with the decision remaining yours

Clients value clear and detailed information, timely answers and regular progress updates. We organise the documentation and coordination work so that the client does not have to manage unnecessary exchanges between multiple parties.

Our role is to research the applicable requirements, explain the available options and provide an honest recommendation. The commercial decision remains with the client.

Where a question falls outside our current knowledge or service scope, we do not guess or provide misleading assurance. We verify the requirement, involve the relevant technical resource where necessary and return with a properly considered response.

International coordination

International coordination experience

Our team has worked with clients and manufacturers located across Germany, France, the United States, Canada, Australia, China, Taiwan, Malaysia, South Korea, Japan and other international markets.

We understand that overseas projects require more than application filing. They require clear communication between the manufacturer, Indian representative, laboratory and regulatory process. Standix Global keeps responsibilities, document requirements and pending actions visible to everyone involved.

Experience that supports the complete BIS journey

Our experience is not limited to identifying whether a product falls under a particular BIS route. We support the wider work needed to prepare and manage a compliance project—from the initial applicability review through testing, documentation, application coordination and post-approval requirements.

The specific support provided depends on the applicable scheme, product, manufacturing location and agreed scope of engagement.

Support for Indian and overseas manufacturers

A domestic manufacturer and a foreign manufacturer may be dealing with the same Indian Standard but face different procedural and operational requirements.

For overseas manufacturers, the project may also require coordination between the factory, Indian representative, laboratory and local regulatory process. Standix Global provides a central point of coordination so that responsibilities, documents and pending actions remain clear across the parties involved.

Why the initial assessment matters

Beginning with the wrong assumption can lead to unsuitable testing, incomplete documentation or an application prepared under the wrong route. These issues may cause avoidable rework and delay.

Our assessment is intended to give your team a clearer starting point. It does not replace the decision of BIS or any other competent authority, but it helps you prepare the project on a better-informed basis.

Regulatory references: This page is informed by official information from the BIS Product Certification Overview, BIS CRS, and BIS FMCS. Applicability and procedures remain subject to current notifications, standards and decisions of the competent authority.

Discuss your BIS requirement.

Share your product details and intended activity in India. We’ll help clarify the route that should be considered.

Request a BIS assessment