ISO 9001: ISO 9001 sets out the standards for a quality management system and is the sole standard in the household that can be licensed to (while this is not a requirement). It can be used by almost any organization, large or small, regardless of its field of activity. There are over one million businesses and organizations in over 170 nations certified to ISO 9001.

This standard is based on several quality management principles such as a strong customer focus, the motivation and consequence of top management, the process approach, and continual progress. These principles are explained in more detail in ISO’s quality management fundamentals. Utilizing ISO 9001 helps ensure that customers get consistent, good-quality merchandise and services, which consequently brings several business benefits.

ISO 31485 is the International Standard, that specifies the quality management systems which are, involved in medical devices.

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

ISO 14001 provides demands with guidance for using that link to environmental systems. Other standards in the family focus on particular approaches such as reports, communications, labeling, and life span evaluation, in addition to environmental issues like climate change.

ISO/IEC 17025 enables laboratories to demonstrate that they function competently and create valid benefits, therefore fostering confidence in their work both nationwide and across the globe.

Additionally, it will help ease cooperation between laboratories and various bodies by producing wider acceptance of results between countries. Evaluation reports and certificates may be taken from one nation to another with no need for further testing, which, consequently, improves international trade.

The results of unsafe food could be severe. ISO’s food safety management standards assist organizations to identify and control food safety risks, at precisely the same time as working with other ISO management standards, including ISO 9001. Applicable to all types of the manufacturer, ISO 22000 supplies a coating of reassurance inside the worldwide food distribution chain, helping goods cross borders and bringing people food that they can trust.

ISO/IEC 27001 is widely known, providing requirements for the information security management system (ISMS), even though there are over just several dozen standards in the ISO/IEC 27000 family. Utilizing them allows organizations of any sort to control the security of assets like financial information, intellectual property, employee details, or information secured by third parties.

To the International Labour Organization, over 7 600 individuals die from work-related injuries or diseases every single moment. That is why an ISO committee of occupational health & safety specialists place to work to develop an International Standard using the potential to save nearly three million lives each year. Structured in a similar approach to other ISO management systems, the approach will be familiar to consumers of standards such as ISO 14001 or ISO 9001. ISO 45001 builds on the success of previous international standards in this area like OHSAS 18001, the International Labour 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 that products are consistently produced and controlled by quality standards. It’s intended to decrease the risks involved with any pharmaceutical manufacturing that may not be eliminated through testing the final product. The main risks are unexpected contamination of merchandise, causing damage to health or even death; wrong tags on containers, which might mean that patients get the wrong medicine; insufficient or too much active component, resulting in ineffective therapy or adverse results.

 GMP covers all aspects of manufacturing; from the beginning materials, premises, and equipment to your training and personal hygiene of personnel. Detailed, written processes are critical for each process that could impact the quality of the completed product. There must be systems to present documented proof that correct procedures are always followed at each step in the manufacturing process – every time a product is made.

 WHO has established comprehensive guidelines for good manufacturing practices. Most countries have formulated their particular needs for GMP according to WHO GMP. Others also have harmonized their requirements, for example in the Association of South-East Asian Nations (ASEAN), at the European Union, and through the Pharmaceutical Inspection Convention.

Vulnerability assessment and penetration testing are the 2 types of tests comprising different strength and total vulnerability assessment. Any cybersecurity Accidents could be recognized with the assistance of these two security testing procedures.

ISO 31000, Risk management — Guidelines, supplies principles, a framework, and a method for managing risk. It can be employed by any organization no matter its dimensions, activity, or business.

Employing ISO 31000 can help organizations increase the chance of achieving objectives, enhance the identification of opportunities and risks and effectively allocate and use resources for risk therapy.

But, ISO 31000 cannot be used for certification purposes but can guide internal or external audit programs. Organizations using it may evaluate their risk management practices using an internationally known benchmark, providing sound fundamentals for successful management and business governance.