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IATF 16949:2016 is a global standard certification for Automotive Quality Management Systems. The International Automotive Task Force (IATF) members collaborated to develop IATF 16949, then submitted to the International Organization for Standardization (ISO) for approval and publication. The document is a common automotive quality system requirement based on ISO 9001 and customer-specific automotive sector requirements.

The IATF 16949 standard emphasizes the creation of a process-oriented quality management system that allows for continuous improvement, preventing defects, and reducing variation and waste in the supply chain. The goal is to efficiently and effectively meet the needs of the customers.

Who Should Apply for IATF 16949:2016 (Automotive)?

The IATF 16949:2016 applies to any organization that produces components, assemblies, or parts for the automotive industry. Anyone involved in the production of materials, assemblies or heat treatment, production or service parts, welding, painting, plating, or other finishing services.

The Benefits of IATF 16949 certification

• An organization can demonstrate its ability to consistently provide products that meet the customer's needs and applicable statutory, regulatory, and product safety requirements.
• Putting the customer first, ensuring that their needs are met consistently, and increasing their satisfaction.
• Increase customer loyalty, add new clients, and expand your business by retaining customers.
• Improve customer satisfaction by using the system effectively.
• Implement systems-improvement processes.
• Helps in declaring your goals clearly and looking for new business opportunities.
• Expand into new markets, as some industries and clients require IATF 16949 certification before doing business.
• Identify and address the risks that your organization constantly faces.
• Work more efficiently to increase productivity and efficiency while lowering internal costs.

How Can QACA Help You?

A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for IATF 16949. Audits are conducted by our certified certification bodies that follow the IATF 16949.

We also help you with: 

• Recognize your customers' current and future needs and expectations.
• Connect the organization's goals to the needs and expectations of its customers.
• Ensure that customer needs and expectations are communicated throughout the organization.
• Plan, design, develop, manufacture, deliver, and support products to meet the needs and expectations of customers.
• Process effectiveness and efficiency

You can request an audit from us to evaluate your organization's performance based on IATF 16949. 

ISO 13485:2016 is a global standard certificate that specifies requirements for a quality management system. Using the certificate, organization must demonstrate its ability to consistently provide medical devices and related services that meet customer and applicable regulatory requirements.

The ISO 13485 standard is an efficient way to meet all of the requirements for a QMS. Adopting ISO 13485 provides a practical foundation for manufacturers to address regulations and responsibilities while also demonstrating a commitment to medical device safety and quality.

Who Should Apply for ISO 13485:2016?

Organizations involved in one or more stages of the life-cycle of a medical device, such as design and development, production, storage and distribution, installation, or servicing, as well as design and development or provision of associated activities (e.g., technical support) can apply for the certificate.

 ISO 13485:2016 can also be used by suppliers or external parties who provide products to such organizations, including quality management system-related services.

The Benefits of ISO 13485:2016

• Rapid and consistent cycle
• Reduced waste
• Process improvement as a system
• Increased customer satisfaction
• Greater credibility and prestige
• Increase the reliability and image of your company

How Can QACA Help You?

A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for ISO 13485:2016. In addition, our certified certification body conducts audits that follow the ISO 13485:2016. 

QACA helps achieve certification that can demonstrate to potential clients that they adhere to best practices and regulatory requirements. We help the company benefit from improved process control and continuous improvement, resulting in continuous ROI.

You can request a certificate from us to evaluate your organization's performance based on ISO 13485:2016.

ISO 3834-2:2003 is a supplement to ISO 9001 requirements, bringing together a comprehensive solution of quality requirements related to welding as well as a Quality Management System. ISO 3834 specifies quality requirements for metallic materials fusion welding processes. It can be used in a variety of situations and applications, including railway vehicles, steel structures, pressure equipment, and so on.

Who Should Apply for ISO 3834-2:2003?

All organizations concerned with fabrication industries, construction companies, i.e., on-site work, repair and maintenance contractors, and manufacturers of products, can apply for the certificate. 

The Benefits of ISO 3834-2:2003

• Get assurance about contract delivery dates
• Increased confidence in the quality of welded products
• Demonstrating the manufacturer's ability to produce the specified products.
• Increasing the level of welding management and ensuring the quality of the product welding.
• Improving the organization international competitiveness
• Raising the product reliability and performance 
• Reducing or minimizing the maintenance costs 
• Eliminating and reducing third-party inspection costs.
• Get trained and knowledgeable suppliers of welded products. 

How Can QACA Help You?

A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for ISO 3834-2:2003. In addition, our certified certification body conducts audits that follow the ISO 3834-2:2003.

You can request a certificate from us to evaluate your organization's performance based on ISO 3834-2:2003.