ISO 9001 sets out the criteria for a quality management system and is the only standard in the family that can be licensed to (even though this isn’t a requirement). It may be used by any organization, large or small, irrespective of its field of activity. There are over one million businesses and organizations in over 170 countries certified to ISO 9001.

This standard relies on several quality management principles such as a strong customer focus, both the motivation and effect of high management, the process approach, and continual progress. These principles are explained in greater detail in ISO’s quality management fundamentals. Using ISO 9001 helps ensure that customers get constant, good-quality products and services, which in turn brings many business advantages.

ISO 31485 is an International Standard, which specifies the Quality management systems that are, involved with medical devices.

ISO 13485 signifies the prerequisites for a comprehensive quality Management system for its design and fabrication of medical devices.

ISO 14001 lays out the standards for the environmental management system and can be certified. It maps a framework that a company or organization can follow to prepare an effective environmental management system.

Designed for any kind of organization, irrespective of its activity or sector, it can assure company management and employees in addition to external stakeholders which environmental impact has been measured and enhanced.

WHAT DO THE STANDARDS IN THE ISO 14000 FAMILY COVER?

The ISO 14000 family of standards are developed by ISO Technical Committee ISO/TC 207 and its various subcommittees. For a full list of published standards in the series visit their standards catalog.

ISO 14001 provides requirements with guidance for using that link to environmental systems. Other standards in the family concentrate on particular approaches like audits, communications, labeling, and life cycle evaluation, in addition to environmental challenges like climate change.

ISO/IEC 17025 enables laboratories to show that they function competently and generate valid results, thereby promoting confidence in their work both nationwide and around the world.

Additionally, it will help facilitate collaboration between laboratories and various bodies by producing broader acceptance of outcomes between countries. Evaluation reports and certificates can be accepted from one country to another with no need for additional testing, which, consequently, enhances international trade.

The effects of unsafe food could be serious. ISO’s food safety management standards help organizations identify and control food safety hazards, at precisely exactly the identical time as working together with additional ISO management standards, such as ISO 9001. Applicable to all types of manufacturers, ISO 22000 provides a layer of reassurance inside the international food supply chain, helping goods cross boundaries and bringing folks food that they can trust.

ISO/IEC 27001 is broadly known, supplying requirements for the information security management system (ISMS), though there are over just several dozen standards in the ISO/IEC 27000 household. Utilizing them enables organizations of any kind to handle the security of assets such as financial information, intellectual property, employee information, or information entrusted by third parties.

According to the International Labor Organization, more than 7 600 people die from work-related injuries or diseases every single moment. That’s why an ISO committee of occupational health & safety specialists set to work to develop an International Standard using the capacity to save nearly three million lives every year. 

Structured in a similar approach to other ISO management systems, the strategy will be familiar to consumers of standards like ISO 14001 or ISO 9001. ISO 45001 builds on the success of earlier international standards in this area such as OHSAS 18001, the International Labor Organization’s ILO-OSH Regulations, assorted federal standards, and the ILO’s international labor standards and conventions.

Good manufacturing practice (GMP) is a system for ensuring the products are consistently produced and controlled by quality standards. It’s designed to decrease the risks involved in any pharmaceutical manufacturing that must not be eliminated throughout testing the final item. 

The key risks are sudden contamination of goods, causing harm to health or even death; wrong labels on containers, which could mean that patients receive the wrong medicine; inadequate or too much active ingredient, resulting in ineffective therapy or adverse outcomes. 

GMP covers all aspects of production; from the beginning materials, premises, and equipment to this training and personal hygiene of employees. Detailed, written processes are crucial for every process that could impact the quality of the final product. 

There must be systems to provide documented evidence that proper procedures are followed at each step in the manufacturing process – whenever a product is made. WHO has established comprehensive guidelines for good manufacturing practices. 

Most nations have formulated their own needs for GMP based on WHO GMP. Others have harmonized their requirements, for example in the Association of South-East Asian Nations (ASEAN), in the European Union, and throughout the Pharmaceutical Inspection Convention.

Vulnerability assessment and penetration testing are the two types of tests comprising different potency and total vulnerability assessment. Any cybersecurity Accidents could be recognized with the support of both of these security testing methods.

ISO 31000, Risk management — Guidelines, supplies principles, a framework, and a process for handling risk. It may be used by any organization no matter its size, activity, or business.

Employing ISO 31000 can help organizations raise the odds of achieving goals, improve the identification of opportunities and risks and effectively allocate and utilize funds for risk therapy.

But, ISO 31000 cannot be used for certification purposes but does provide advice for external or internal audit programs. Organizations using it can compare their risk management practices with an internationally known benchmark, providing sound fundamentals for effective management and business governance.