I'm a title

Product Certification & Qualifications Services

Product certification – also known as product qualification – is the process of certifying that a product has successfully passed performance tests, quality assurance checks, and complies with specific qualification criteria. These criteria are typically defined in contracts, regulations, standards, or certification schemes across industries.

As an international standard service provider, we offer expert advisory and consultancy services to help businesses achieve smooth and reliable product certification. Whether you are a manufacturer, importer, or exporter, our services ensure that your products are recognized for safety, quality, and compliance in both domestic and global markets.

Our Expertise Covers:

End-to-end guidance on certification schemes across multiple industries
Regulatory requirement mapping and compliance strategy
Product testing coordination with accredited laboratories
Documentation, technical dossier preparation, and submission
Liaison with certification bodies and authorities
Post-certification compliance and renewals

Why Choose Us?

Global Recognition – Advisory aligned with international standards and certification bodies
Industry Coverage – Medical devices, pharmaceuticals, consumer goods, electronics, textiles, and more
Compliance Assurance – Minimized risks of rejection, delays, or regulatory non-compliance
End-to-End Support – From initial assessment to certification grant

✅ With our comprehensive consultancy approach, we make the product certification journey seamless, enabling your business to access regulated markets worldwide with confidence and credibility.

CE Marking Certification

Directive under service scope:
1. Low Voltage (LVD)
2. Machinery (MD)
3. Construction Product (CPR)
4. Personal protective Equipment (PPE)
5. Medical Device (MDD)
6. In-vitro Diagnostic Medical Device
7. Measuring Instrument (MID)
8. Electromagnetic Compatibility (EMC)
9. Gas Appliances (GAR)
10. Chemical Substances (REACH)
11. General Product Safety
12. Toy Safety
13. Radio Equipment (RED)
14. Pressure Equipment (PED)

U.S. Food & Drug Administration

"Achieve seamless access to the U.S. market with our expert FDA consultancy and advisory services. From regulatory strategy to product certification, we guide businesses through every step with accuracy, compliance, and confidence."

Following product groups covered under this regulation:

1. Food

2. Drugs

3. Medical Devices

4. Radiation-Emitting products

5. Vaccines, blood and biologics

6. Animal and Veterinary

7. Cosmetics

8. Tobacco Products

CUTR/Gost-R Certification

Certifies quality of actually supplied goods and their compliance with contractual terms. A quality certificate contains a profile of goods or confirms their compliance with certain standards or specifications of a delivery order. A certificate of compliance is intended for certification of goods produced by Russian companies or shipped to Russia by an importer-company. A certificate of compliance can be issued for a batch of goods and on a series production. In the former case a certificate is legalized for a company engaged in supplying goods to the Russian market. Its validity varies with terms of a sale contract. In the latter case a foreign manufacturer of supplied goods is both an applicant and a recipient of a certificate. This type of a certificate is valid for a period identified in a certification document. Certification is carried out by our specialists on production premises of a company seeking certification of goods it manufactures. On the basis of results obtained during testing samples of goods in a laboratory an appropriate certificate of series production compliance is issued.
There are cases where GOST certificate is issued when documents like: a hygienic report, a veterinary certificate, fire safety certificate, etc. are available. These all mean that we must receive all these documents for you before.

ISI, CSR, FMCS, Scheme-X

The Bureau of Indian Standards (BIS) is the statutory body under the Government of India, responsible for product certification and standardization. BIS offers various certification schemes such as ISI, CRS, FMCS, and Scheme-X, covering a wide range of product disciplines.

As these certifications are mandatory for accessing the Indian market, compliance is crucial for both domestic manufacturers and foreign exporters.

At EQR, we provide end-to-end consultancy services for BIS product certification – from documentation, application filing, product testing, and liaison with BIS, to successful grant of certification. Our expertise ensures a smooth, hassle-free process, helping your products meet Indian regulatory requirements with confidence.

CDSCO Registration

The Central Drugs Standard Control Organization (CDSCO), under the Ministry of Health & Family Welfare, Government of India, is the national regulatory authority responsible for the safety, efficacy, and quality of medical devices, in-vitro diagnostics (IVDs), cosmetics, and pharmaceuticals.

Navigating CDSCO regulations can be complex, and non-compliance may delay market entry or restrict business operations.

At EQR, we specialize in providing end-to-end consultancy and advisory services for CDSCO approvals and certifications. Our experts assist clients with:

Medical Devices – Classification, registration, import licensing, and regulatory submissions.
In-Vitro Diagnostics (IVDs) – Approval and compliance support for diagnostic kits and reagents.
Cosmetics – Import registration, labeling compliance, and approval for market launch.
Drugs & Pharmaceuticals – New drug approvals, clinical trial permissions, and regulatory filings.

Our Services Include:

Regulatory strategy & compliance roadmap
Documentation, dossier preparation, and submission
Liaison with CDSCO & regulatory authorities
Support for testing, audits, and inspections
Post-approval compliance and renewals

✅ With our domain expertise and hands-on experience, we help manufacturers, importers, and distributors achieve timely CDSCO approvals, ensuring seamless market access in India.

UL Green Guard

UL GREENGUARD Certification is a globally recognized product certification program that ensures materials and products meet strict chemical emissions limits, contributing to healthier indoor air quality. Products bearing the GREENGUARD mark demonstrate compliance with rigorous performance and safety criteria, helping manufacturers, architects, and consumers build sustainable, eco-friendly environments.

As an international consultancy and advising service provider, we specialize in guiding businesses through the UL GREENGUARD certification process with end-to-end support. Our services are designed to help you achieve compliance efficiently while enhancing your product’s market acceptance and brand value.

Our Expertise Includes:

Understanding certification requirements & qualification criteria
Gap analysis and compliance roadmap development
Coordination with accredited testing laboratories for VOC emissions testing
Preparation and submission of technical documentation
Liaison with UL and certification authorities for smooth approvals
Renewal support and ongoing compliance monitoring

Benefits of GREENGUARD Certification:

Validates product safety for indoor environments
Builds trust with customers and stakeholders
Supports LEED and other green building credits
Enhances global market access and competitiveness

✅ With our specialized consultancy and advisory services, we ensure your products meet the highest standards of indoor air quality and sustainability, making them GREENGUARD certified and market-ready.