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The BRC Food, Packaging S&D, and A&B Certification is the global standard for food safety that specifies how processed foods and other goods should be created or prepared by retailer-branded foods, foodservice organizations, caterers, or manufacturers. By ensuring the consistency of quality, safety, and operational principles, BRC Global Standards provide confidence across the whole supply chain.
The BRC Food, Packaging S&D, and A&B Certification standard was developed for companies that purchase, import, or distribute products in the food and food packaging supply chain. This standard's methods ensure product safety, quality, and legality.
A Quality Austria Central Asia certificate verifies that internal corporate processes have been checked and are in compliance with the relevant standard for BRC Food, Packaging S&D, and A&B. Audits are conducted by our certified certification bodies that follow the BRC Global Standards.
You can request a certificate from us to evaluate your organization's performance based on BRC Food, Packaging S&D, and A&B Certification.
Related Certificates
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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was popularised in the 1960s with the release of Letraset sheets containing Lorem Ipsum passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum.
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.
