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Related Certificates
Food Safety System Certification 22000 (FSSC 22000) is an internationally recognized, ISO-based certification process for food safety auditing and certification in the food and beverage manufacturing industry.
FSSC 22000 is based on the ISO 22000, ISO 22003, and technical specifications for sector prerequisite programs (PRPs), created after long, extensive and open consultation with a wide range of stakeholders.
Anyone who desire to upgrade their certification to a GFSI recognized Standard, FSSC 22000 is the next logical step.
FSSC 22000 can be used by organizations in the food/feed supply chain of any size or complexity. Makers of various types of food and beverages, ingredients/additives, pet and animal feed manufacturers, and packaging manufacturers are all included.
A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for FSSC 22000 Certification. Our certified certification body conduct an audit that follows the FSSC 22000 Certification.
You can request a certificate from us to evaluate your organization's performance based on FSSC 22000 Certification.
ISO 9001 is a global standard certification that guides the requirements for a quality management system (QMS). Organizations use ISO 9001:2015 standard to demonstrate their ability to consistently provide products and services that meet the needs of their customers and the requirements of the regulatory authorities. It is the most widely used standard in the ISO 9000 series and the only one to which organizations can certify.
The International Organization for Standardization (ISO), an international organization consisting of more than 160 national standards bodies first published the ISO 9001 in 1987. In September 2015, the most recent version of ISO 9001 was released.
ISO 9001:2015 is applicable to any organization, no matter its size or industry. More than one million organizations from over 160 countries have used the ISO 9001 standard requirements to improve their quality management systems.
A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for ISO 9001:2015. Audits are conducted by our certified certification bodies that follow ISO 9001:2015. We help you create and implement a quality management system based on the most recent ISO 9001 standard principles.
ISO 41001:2018 is a global standard certificate by the International Organization for Standardization that sets forth guidelines for facility management. It follows the same structure as other ISO standards, such as ISO 45001 (Occupational Health and Safety) and ISO 50001 (Energy Management), with the exact core text, definitions, and terms.
The standard aims to help organizations demonstrate efficient and effective FM, pursue consistency when defining FM requirements, and achieve sustainability. It standardizes FM concepts and requirements so that organizations of all kinds can benefit from it.
It is not sector-specific and intended to apply to all organizations or parts of organizations, public or private, regardless of the organization's type, size, nature, or geographical location.
ISO 41001's core objectives assist organizations in gaining the following advantages:
A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for ISO 41001:2018. In addition, our certified certification body conducts audits that follow the ISO 41001:2018.
QACA helps your organization gain the confidence of stakeholders by recognizing various stages and offering comprehensive evaluations and reports.
You can request a certificate from us to evaluate your organization's performance based on ISO 41001:2018.
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.
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.
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.