ISO 50001 | Energy Management Systems

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ISO 50001 is a global standard certification whose primary goal is to provide the efficient use of an Energy Management System. Like some other common ISO standards, the standard is based on a management system model of continuous improvement.

The certification requires a company to develop an energy policy, set goals to meet the policy, use data to meet the goals, measure policy effectiveness, and continuously improve the policy.

Adopting ISO 50001 is critical for establishing a more systematic and sustainable approach to energy management within a facility. When you comply with the standard, it demonstrates that your organization has implemented a sustainable energy management system.


Who Should Apply for ISO 50001?

The standard provides organizations, ranging from large retailers to smaller manufacturers and small businesses, with the opportunity to become more resilient to energy costs and availability.


The Benefits of ISO 50001

  • • Enhanced tender opportunities by demonstrating your environmental credentials.
  • • Helping organizations gain external credibility for their energy-saving efforts.
  • • Provides a better understanding of the relationship between predictable energy demand and supply
  • • Increasing profitability while minimising energy costs
  • • Recognizing and managing the risks associated with your future energy supply.
  • • Measure and monitor energy consumption to determine where efficiency can be improved.
  • • Enhancing overall performance by reducing energy consumption and costs.
  • • Reducing carbon emissions while meeting government desired goals.


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 50001. In addition, our certified certification body conducts audits that follow the ISO 50001.

You can request a certificate from us to evaluate your organization's performance based on ISO 50001. 

Related Certificates


ISO 13485 is a global standard certificate that specifies requirements for a quality management system. Using the certificate, the 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?

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 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

  • • 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. In addition, our certified certification body conducts audits that follow the ISO 13485. 

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.


We’re in a digital economy where data is more valuable than ever. It’s the key to the smooth functioning of everything from effective administration to businesses. Without it, progress would halt. You probably have heard the expression "data is the new oil." In fact, data today is fuelling an increasing number of businesses. Personalized customer experiences, automated marketing messages, and science-driven insights all depend on the quality and volume of the information. Firms are eager to collect data. Regulators, on the other hand, are working hard to protect the privacy and safety of individual and organizational data.
Businesses often face challenges globally as they aim to comply with data privacy regulations like Europe's General Data Protection Regulation (GDPR) & other local regulations. In India currently, data privacy is in an amorphous state and soon with the adoption of the Digital Personal Data Protection Act, 2022 stringent rules and regulations will be in place to manage information privacy. The French data protection authority, the CNIL, has recently recognized the interest of the ISO/IEC 27701:2019 standard for data protection. To demonstrate organizational compliance with data privacy and security there are various management systems that can be adopted and one of them is ISO 27701.

ISO 27701:2019 is the first global privacy management standard. It sets out requirements relating to the implementation of a Privacy Information Management System (PIMS). The ISO 27701 standard serves to demonstrate compliance with data protection regulations and represents an extension of the well-known ISO 27001. Both standards and the combined management system are based on the principles of confidentiality, integrity, and availability of data and information. The conformity with the standard’s requirements is certifiable & businesses can get certified by adoption and implementation of the requirements of the standard.  The ISO/IEC 27701:2019 proposes a set of additional requirements and guides dedicated to the protection of personal data in extension to ISO 27001.

Risk-based Approach

The ISO/IEC 27701 encapsulates a risk management process defined by ISO as the “organized application of management policies, procedures, and practices to the activities of communicating, consulting, establishing the context, identifying, analyzing, evaluating, treating, monitoring and reviewing risk.’ In the ISO/IEC 27701:2019, the risk management process aims to assess and address the data security risks associated to the loss of confidentiality, integrity, and availability of personal data.

Certification Process

This is typically a two-stage process consisting of a system appraisal and an initial assessment, the duration of which is dependent on the size and nature of your organization.
The successful demonstration by an organization against the requirement of the ISO 27701 standard during the third-party assessment by the Conformity body will result in certification. The certification cycle is of 3 years with which the first year being for Readiness and Certification Audit. In the following 2 years, annual Surveillance audits are conducted to assess compliance with the existing system requirements and to capture the changes, if any.

Need and Benefits of adopting ISO 27701

• Ensures legal and regulatory compliance.  
• Minimizes the risk of data privacy breaches and hence the potential consequences.  
• Building trust with existing stakeholders and potential customers. 
• Defines roles and responsibilities clearly 
• Offers a structured framework that could be used by businesses to streamline their internal personal data processing activities.
• ISO 27701 satisfies the demand from your customers and suppliers for managing the data privacy requirements. 

How can we help?

Quality Austria offers the Certificate for Privacy Information Management Systems as per ISO 27701 standard – in the form of an extension to ISO 27001. Our assessors are qualified professionals with sector-specific information security and IT experience that matches your business needs, ensuring an effective audit of your system. Our certification mark is accepted worldwide, making it a demonstration tool for your system to showcase compliance with data privacy practices.
For any query or support, write to us at:


ISO 9001 is a global standard certification that guides the requirements for a quality management system (QMS). Organizations use ISO 9001 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.

Who Should Apply for ISO 9001 Certifications?

ISO 9001 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.

The Benefits of ISO 9001 Certification

  • • Increase in profitability and market share
  • • Saving time because of better resource management
  • • Process integration and process automation reduce the need for manual labour.
  • • Using data and evidence to inform decision-making improves organizational efficiency and effectiveness.
  • • Minimal or elimination of recurring issues and anomalies
  • • Improving the brand image and credibility of the organization


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 9001. Audits are conducted by our certified certification bodies that follow ISO 9001. We help you create and implement a quality management system based on the most recent ISO 9001 standard principles.

You can request an audit from us to evaluate the performance of your QMS against the most recent ISO 9001 standard.


IATF 16949 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 (Automotive)?

The IATF 16949 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.