Quality Mark Certification is a leading certification body specializing in ISO standards.
We help organizations across industries achieve excellence in quality, safety, environmental responsibility, and information security through internationally recognized ISO certifications. Our mission is to empower businesses to build trust, enhance performance, and gain competitive advantage in the global market.
Founded in 2019, we specialize in enabling organizations of all sizes—from ambitious startups and growing SMEs to large enterprises—to build reliable management systems that meet international ISO standards, enhancing quality, safety, environment, information security, and operational credibility.
Guiding organizations worldwide toward sustainable quality excellence, integrity, and stakeholder trust.
To be the most trusted and dependable partner for ISO certification – enabling organizations to meet and exceed global standards for quality, safety, environment, integrity, and continual improvement in their operations.
Empowering enterprises worldwide with accredited audits, globally recognized certifications, and fast-track compliance. Click any standard below to view complete requirements and audit roadmaps.
Ensures consistent product quality, optimizes operational workflows, and builds client credibility across global supply chains.
Framework for corporate sustainability, controlling industrial waste, reducing energy costs, and statutory compliance.
Proactively eliminates workplace hazards, prevents occupational injuries, and promotes workforce health and safety.
Protects critical intellectual property, customer financial data, IT assets, and cloud infrastructure against cyber threats.
Specialized standard specifying quality system requirements for medical device design, manufacturing, and distribution.
Comprehensive standard integrating HACCP principles to prevent foodborne contamination across processing and packaging.
Mandatory conformity mark verifying products meet high European health, safety, and environmental protection standards.
Ensures electrical and electronic equipment is free from restricted hazardous substances like lead, mercury, and cadmium.
Guarantees products are consistently produced and controlled according to quality benchmarks appropriate for intended use.
Specialized certification verifying adherence to World Health Organization guidelines for pharmaceutical manufacturing.
Systematic preventative approach to biological, chemical, and physical hazards in food handling, storage, and distribution.
Guidance through US FDA establishment registration, medical device listings, cosmetics, and food facility requirements.
Connect directly with our accredited lead auditors for gap analysis, document preparation support, and a transparent fixed quote with no hidden fees.
We provide full-lifecycle ISO certification support tailored to your industry, scale, and operational requirements:
| Service | Description & Implementation Scope | Outcome |
|---|---|---|
|
Gap Analysis & Planning
|
Assess current management systems and workflows; pinpoint non-conformities and identify strategic areas of improvement. | Readiness Check |
|
Consulting & Implementation Support
|
Guidance in documentation, process design, policies, operational controls, and alignment with selected ISO standard requirements. | Seamless Alignment |
|
Training & Awareness
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Interactive workshops and courses for senior management, core implementation teams, and internal auditors. | Skill Building |
|
Third-Party Audits & Certification
|
Independent audits conducted with impartiality, technical rigor, and formal issuance of accredited ISO certificate upon verification. | Global Credibility |
|
Surveillance & Reassessment
|
Periodic reviews and annual audits to ensure management standards are continually maintained, refined, and improved. | Continual Growth |
Accredited by relevant national/international bodies; fully compliant with ISO/IEC 17021, maintaining total impartiality and transparency.
Team of certified auditors with deep domain knowledge and cross-industry practical experience across diverse operations.
We don’t do “one size fits all”—we adapt seamlessly to your industry, scale, operational pace, and regulatory demands.
Deep understanding of international standard requirements combined with localized regulatory knowledge and statutory compliance.
Rapid turnarounds, clear communication, and streamlined auditing schedules without compromising technical rigor.
Pre-audit gap analysis, executive training workshops, ongoing guidance for implementation, and a strong focus on long-term partnerships.
A clear, disciplined, and rigorous methodology designed to guide you smoothly to accredited certification:
Understanding your business, organizational scope, operational objectives, and target ISO standards.
Assessing current practices relative to ISO standards and determining what you already have vs. what is needed.
Providing structured guidance on documentation, quality policies, process workflows, and internal management systems.
Guiding and training teams for compliance, equipping staff with internal auditing and operational readiness.
Conducting independent third-party audits with technical impartiality and rigor; issuing the ISO certificate on success.
Conducting periodic reviews and surveillance follow-ups to ensure ongoing compliance and continual improvement.
The foundational pillars that guide our auditors, our culture, and our partnerships:
Upholding honesty, ethics, and strict impartiality in all dealings and assessments.
Delivering high quality, consistent, and value-added certification services.
Your continuous improvement, operational compliance, and satisfaction matter most.
Keeping up with international standard updates, regulatory changes, and emerging industry best practices.
Promoting environmental protection, social accountability, and occupational safety stewardship across every engagement.
We serve a diverse portfolio of clients across key industrial sectors, ranging from innovative startups and SMEs to prominent large enterprises:
Our goal is to enable every organization to meet global standards, elevate stakeholder trust, and unlock international market access.
We are committed to upholding the highest standards in our own operations, maintaining & continually improving:
Real feedback from organizations that achieved accredited ISO certifications through our body:
"Our ISO 9001 and ISO 14001 certificates are valid and accepted in over 150 countries. The audit team was transparent and highly professional."
"Exceptional experience achieving ISO 27001 information security certification. Fast turnaround time and great support from the auditors."
"Clear guidance during the initial gap analysis and audit phase. Quality Mark Certification is our long-term partner for management standards."
"Excellent audit rigor and seamless documentation review for our medical devices standards. Highly recommended certification body!"
Request a free initial consultation, gap analysis roadmap, or quotation.
Kh. No. 47/7, Street No. 6, Kaushik Encalve, Delhi- 110084
10:00 A.M. to 6:00 P.M.
Monday – Saturday