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PRODUCT CERTIFICATION • BIS • ISI • CE • COMPLIANCE

Find the Right Product Certification & Compliance Route for Your Product.

Not sure whether your product needs BIS, an ISI-mark related licence, CE marking or another regulatory/compliance route? OINDC helps manufacturers and businesses identify the applicable requirement, map the product to relevant standards/regulations, prepare documentation and coordinate the certification or conformity-assessment process.

Product Mapping • Standard/Regulation Review • Documentation • Testing Coordination • Application Support
OINDC Product Certification Review and Testing Coordination

Important Statement: OINDC provides consulting, documentation, testing coordination, and compliance-readiness support. The competent regulatory authority, certification body, or notified/conformity-assessment body makes the formal certification/approval decision.

Regulatory Pathways

Which Product Certification Route Do You Need?

Select the certification or conformity pathway relevant to your target market and product type.

Indian Compliance

BIS Registration & Licensing

Determine whether your product falls under mandatory BIS registration, CRS (Compulsory Registration Scheme), or Quality Control Orders (QCOs).

Check BIS Requirement
Product Marking

ISI Mark Scheme

Understand Indian Standards (IS), factory quality control readiness, sampling rules, and licensing requirements for ISI marking.

Check ISI Applicability
European Union

CE Marking & EU Directives

Identify applicable EU directives/regulations, harmonized standards, technical file preparation, and Declaration of Conformity routes.

Check CE Requirement
Specialized Compliance

Electrical, Machinery & Pressure Equipment

Navigate technical safety standards for machinery, low-voltage equipment, toys, or industrial components.

Discuss Specialized Product
Global Trade

Export Market Product Compliance

Map product compliance requirements for specific target countries, import barriers, and destination regulations.

Check Export Requirement
Lab Support

Lab Testing & Technical File Support

Coordinate testing parameters with recognized laboratories and compile structured technical files for audit readiness.

Request Lab & Doc Support
Indian Standards

BIS & ISI-Mark Support

OINDC helps businesses determine whether their products fall under applicable Indian Standards, mandatory Quality Control Orders (QCOs), or BIS certification schemes.

✓ Map product categories to Indian Standards (IS) and QCO applicability
✓ Review factory testing and quality control equipment readiness
✓ Coordinate sample testing with NABL/BIS accredited laboratories
✓ Prepare technical documentation and application submission files
European Union

CE Marking & EU Compliance

CE marking requires demonstrating product conformity with applicable EU directives and regulations before placing products on the European market.

✓ Identify applicable EU Directives (LVD, EMC, MD, RoHS, etc.)
✓ Determine self-declaration vs. Notified Body requirement routes
✓ Organize Technical Files (risk assessments, drawings, test reports)
✓ Guide EU Declaration of Conformity and product labelling requirements

Product Certification & Compliance Journey

From product identification to ongoing compliance surveillance.

01

Identification

Product details, models, and destination markets.

02

Mapping

Identify applicable standards, QCOs, & Directives.

03

Route Check

Confirm mandatory vs. voluntary certification pathways.

04

Gap Assessment

Evaluate product design, docs, and factory controls.

05

Testing Plan

Coordinate testing parameters with suitable labs.

06

Documentation

Compile technical files, test reports, & drawings.

07

Application

Submit files to authorities or notified bodies.

08

Closure

Address observations and audit findings.

09

Marking

Guide compliant product labelling and marking.

10

Compliance

Support ongoing renewals & technical changes.

Why Product Certification Applications Get Delayed

Avoid common pitfalls that slow down market entry and registration.

❌ Wrong Standard Selected

Applying the wrong Indian Standard or EU directive results in rejected test reports and wasted expenditure.

❌ Testing Scope Mismatch

Conducting laboratory testing that omits mandatory parameters required by regulators or Quality Control Orders.

❌ Incomplete Technical Files

Submitting inconsistent drawings, inaccurate bills of materials, or weak factory quality-control documentation.

Compliance Assessment Form

Check Certification Requirements for Your Product

Share your product details, manufacturing location, and target market. OINDC will perform a preliminary requirement assessment and outline the compliance route.

Check Product Certification Requirement

Product Certification FAQ

Common regulatory questions from manufacturers and importers.

Does every product require BIS certification in India?

No. BIS registration or licensing applies to products specified under Indian Standards, mandatory Quality Control Orders (QCOs), or voluntary certification schemes. Applicability must be verified against current official orders.

Does every CE-marked product require a Notified Body?

No. Whether a Notified Body is legally required depends on the specific EU directive and risk classification of your product. Many low-risk products permit manufacturer self-declaration with a valid technical file.

Can OINDC guarantee product approval or certification?

No. OINDC provides expert consulting, technical file assembly, testing coordination, and readiness support. The competent regulatory authority or designated certification body makes the formal compliance decision.

How long does product certification take?

Timelines vary based on product complexity, mandatory testing duration, technical documentation readiness, laboratory availability, and authority audit schedules.

Move from Uncertainty to a Verified Product Compliance Roadmap.

OINDC helps manufacturers map applicable standards, organize testing and technical files, and coordinate the certification process.