At Quality Asia Certification, we offer ISO 21856:2022 certification services to support organizations involved in the design, production, and distribution of assistive products for persons with disabilities. This standard provides a globally recognized framework for ensuring safety, reliability, and performance in assistive technology. With the growing focus on accessibility and inclusion, ISO 21856:2022 plays a vital role in helping companies align with international best practices and legal expectations.
The certification process enhances your product credibility, improves consumer confidence, and opens access to regulated and international markets. Our expert auditors ensure a smooth, compliance-driven certification journey tailored to your organization’s operational needs.
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ISO 21856:2022 is the latest international standard that outlines general requirements and guidance for assistive products used by persons with disability. It covers design principles, safety, risk management, durability, and performance aspects of products such as mobility aids, sensory enhancement devices, and other tools that promote independence and functionality.
This standard ensures that assistive products meet essential safety and usability benchmarks, reducing risks to users and promoting equitable access to technology. It applies to both standalone assistive products and those integrated into broader systems or environments.
As global regulations around accessibility evolve, compliance with ISO 21856:2022 becomes a strategic priority. Governments, healthcare organizations, and NGOs now demand assistive products that conform to internationally recognized safety and quality benchmarks.
By choosing ISO 21856 certification:
ISO 21856:2022 helps organizations strengthen product design and reliability in the assistive technology sector. Key benefits include:
Getting ISO 21856:2022 certified by Quality Asia Certification brings measurable advantages to your business:
✅ Market Expansion: Gain access to global healthcare, rehabilitation, and public sector markets demanding ISO-compliant assistive products.
✅ Risk Reduction: Minimize liability and reputational damage by ensuring product safety and regulatory compliance.
✅ Brand Differentiation: Stand out in the assistive technology market by showcasing internationally certified products.
✅ Tender Eligibility: Increase qualification for government and institutional procurement bids.
✅ Customer Trust: Boost confidence among users, caregivers, hospitals, and NGOs.
✅ Compliance Assurance: Stay ahead of future regulatory updates and disability inclusion mandates.
Top management commitment while practicing and accomplishing the standard is the key to success.
Keeping staff informed about the ongoing practices, a well-communicated plan would increase the motivation and zeal of working in them.
Making sure that the various departments of the organization work as a team for the benefit of the organization and customers as well.
Review systems, policies, processes, and procedures for a smooth working of QMS.
Speaking to customers & suppliers while getting feedback & working on improvements.
Training staff carrying out the internal audits with the opportunity for improvement.
Celebrate your achievement and use the QualityAsia Assurance Mark on your literature, promotional material, and website.
Ensure continuous improvement by regularly reviewing and updating your quality management practices.
Promote a culture of quality by encouraging innovation, accountability, and employee involvement at every level of the organization.
QualityAsia always vanguard in the auditing and governing of internationally acclaimed standards practices. At QualityAsia, we focus on driving the success of our clients through creating excellence with our trained professional auditors. The content of our service provision, comply with international certification rules defined by the accreditation bodies without burning a hole in your pocket. We will take you through the journey of audits with our best kept audit practices, viz.:
Drawing out the scrutiny on various aspects of the previously done audits on effectiveness while reviewing the various processes and control of the operations in the QMS and finally going for the recertification.