Every regulatory question, answered in one place.

BIS CRS (Compulsory Registration Scheme, formally “Scheme II”) is the mandatory registration route for notified electronics and IT products, spanning 60+ categories including laptops, mobile phones, power banks, LED products, routers and monitors. It runs on self-declaration and lab test reports, with no mandatory factory inspection.

ISI Domestic (Scheme I) applies when your factory is based in India and involves a factory audit plus ongoing surveillance. ISI FMCD (the Foreign Manufacturers Certification Scheme) is the same ISI mark for factories outside India, audited abroad through an Authorised Indian Representative.

BIS has tightened traceability between registered models, test reports and market samples, brought standalone hard disk drives under mandatory registration from November 2026, and is migrating many IT/AV categories to the newer IS/IEC 62368-1:2023 safety standard.

No — CRS runs on self-declaration and accredited lab test reports, unlike ISI (Scheme I) or FMCS, which both require a factory audit.

It depends on your certification pathway — BIS CRS typically needs electrical safety testing, WPC/ETA needs RF testing, and medical devices need biocompatibility testing. We map the exact tests required once we know your target certification.

We coordinate testing through NABL/ILAC-accredited third-party laboratories matched to your product category, rather than running an in-house lab — this keeps results independently credible to regulators.

Yes — client specification testing is a standard offering alongside standards-based testing, useful when a buyer has additional requirements beyond the regulatory minimum.

It varies significantly by test type and lab queue — simple electrical safety tests can turn around in days, while comprehensive EMC or medical device testing can take several weeks. We build testing time into your overall certification timeline upfront.

Not necessarily to register as an OEM, but you’ll typically need an Indian entity — your own or an appointed reseller’s — to fulfil and deliver orders, since transactions run on Indian GST and banking rails.

A mandatory third-party review of an OEM’s manufacturing capability, quality systems and financial standing, conducted through RITES Ltd, required before certain OEM listings are approved on GeM.

OEM registration lets you list under your own brand and issue authorization codes to distributors. Reseller registration is for entities selling another brand’s products using an OEM-issued code — the standard route for overseas manufacturers without an India entity.

No — GeM listing and certifications like BIS or WPC are entirely separate requirements. Your product still needs whatever certification applies to it regardless of sales channel.

Yes. Trademark rights are territorial, so a foreign registration grants no automatic protection in India — you’ll need a separate Indian filing.

“TM” can be used the moment you’re using a mark commercially, even pre-registration. “®” may legally only be used once the mark is formally registered with the Trade Marks Registry.

During journal publication, any third party can file an opposition. We handle the counter-statement and represent you through proceedings — most applications that reach this stage still register, though the timeline extends.

Before, wherever possible — public disclosure before filing can jeopardize novelty, a core patentability requirement. A provisional filing is a fast way to lock in a priority date ahead of launch.

Yes. BIS certifies technical safety; LMPC governs what’s declared on the packaging (MRP, net quantity, origin). They run on entirely separate rules, and one doesn’t substitute for the other.

In most cases yes — a compliant sticker declaring the required India-specific information is an accepted route, provided it’s legible, permanent and doesn’t obscure existing information.

Yes — packaged goods sold online are subject to the same mandatory declarations as products sold in physical retail.

Importer registration is typically one-time for pan-India sale, but every new product variant or label redesign needs to be re-checked against current declaration requirements before launch.

Yes. EPR obligations apply to producers, importers and brand owners alike — the rules don’t exempt importers, since responsibility follows whoever places the product on the market.

No — e-waste, battery, plastic, tyre and used-oil EPR are governed by separate rules with their own registration and reporting, even for a single product.

A Producer Responsibility Organisation handles the physical collection and recycling logistics on your behalf. Most brands work with a PRO rather than building in-house infrastructure.

Registration itself is typically one-time per category, but it comes with an ongoing obligation — annual targets to meet and yearly returns to file for as long as the product stays on the market.

No — MOEF permission is an additional requirement on top of standard DGFT and customs documentation.

Yes, in most cases — samples up to 1000 grams or 1000 millilitres imported for testing or R&D are exempt from the full permission requirement.

No — MOEF permission only ever covers material entering India for recycling, reuse, refurbishment or co-processing. Import for disposal is prohibited outright, regardless of category.

You’re required to maintain records in Form 3 and file an annual return in Form 4 with the State Pollution Control Board, typically by June 30 following the fiscal year.

Effective April 1, 2026, Basic Registration now covers turnover up to ₹1.5 crore (up from ₹12 lakh), State License covers ₹1.5 Cr–₹50 Cr, and Central License applies above ₹50 crore — all significantly higher than before.

Yes — food importers require a Central License regardless of turnover, since import carries additional regulatory oversight.

Generally yes. FSSAI approval is tied to the specific business premises, not the brand, so each kitchen, outlet or warehouse typically needs its own registration assessed on that unit’s activity.

In most cases, Basic Registration, provided turnover stays under ₹1.5 crore and the business operates from a single state.

Generally no — ISO standards certify your management systems, not your product’s legal right to be sold. That said, many GeM tenders and B2B buyers treat a relevant certificate as a practical prerequisite, and CDSCO’s medical device pathway specifically expects ISO 13485.

ISO 9001 (Quality) suits almost any business. ISO 14001 (Environment) and 45001 (Safety) matter most for factories. ISO 13485 is medical-device-specific, 22000 covers food safety, and 20000-1 applies to IT service management.

We work as your implementation partner, preparing documentation and coordinating the certification audit — but the audit itself is always conducted by an independent accredited certification body, which is what gives it credibility.

First-time certification typically takes a few weeks to a few months depending on process maturity. Certificates run on a 3-year cycle, with annual surveillance audits in between.

No — it’s a category label meaning these sit outside India’s mandatory schemes (BIS, WPC, CDSCO). Your product can be fully compliant in India while still needing one of these for a specific export market.

Yes, if exporting. BIS CRS only confirms Indian compliance — FCC and RoHS are separate, destination-market-specific certifications for the US and EU.

It comes down to product category and target market — electronics exporters to the US/EU typically need FCC and RoHS; food exporters to the Gulf typically need HACCP and HALAL.

It varies — some are tied to a product model and don’t expire unless the design changes, while others like HACCP and Organic require periodic re-audits.

IEC is the baseline DGFT registration that makes you eligible to trade at all. The AD Code, issued by your bank, is what customs needs to process your specific shipping bills — you need the IEC first.

No — DSCs are typically valid for one to three years and need renewal. Since many other filings depend on a valid DSC, we track its expiry alongside your other registrations.

They serve different purposes — Udyam establishes general MSME eligibility, while NSIC’s Single Point Registration specifically unlocks tender fee waivers and EMD exemptions. Most MSEs pursuing government tenders hold both.

Yes, a common growth step — it requires fresh incorporation as the new entity type and transferring assets and registrations across, so it’s worth planning early if you expect to scale.

Share your product category, core technology and target launch date through our contact form. We map every applicable regulation — across all 11 categories above — into a single compliance blueprint before any filing begins.

It depends entirely on the product. Simpler single-certification products can clear in weeks; complex electronics needing BIS, WPC and EPR together commonly take several months. We sequence approvals by dependency so unrelated ones don’t wait behind each other.

Yes — specifications and business details are used solely to process your filings, and we’re glad to sign an NDA before deeper technical review if required.

We monitor notifications relevant to your registered products — like the 2026 FSSAI threshold changes or BIS’s IS/IEC 62368-1 migration — and flag renewal or re-testing needs before they become compliance gaps.