ISO 9001 is a globally accepted identification mark for qualified standards of quality administration. The International Standard Organization, that is recognized by more than 120 nations as the jurisdiction in establishing quality standards for products and services.

ISO 13485 Certification is for Quality control systems for medical instruments is an International Organization for Standardization, whose purpose would be to establish quality standards for pharmaceutical, biotechnological and generic drug products. The primary goal of ISO is to set quality standards for drugs, generic drugs, and surgical materials and equipment which are utilized by healthcare and industrial businesses in the production of medications, devices, and equipment. 

The organization sets quality goals, quality management measures, quality control systems, performance data specifications, and labeling or packaging needs. This international standard has been accepted by different governments globally. As of the writing of this article, ISO has 27 member states and is expanding rapidly in all areas of the pharmaceuticals business.

ISO 14001 is the international Standard for developing and implementing a hazardous waste management system. ISO 14001 was established in 1996 to help facilitate the compliance of resources of poisonous wastes. Its objective is to establish a uniform system of technology principles and rules required for managing such wastes. The standard is always upgraded through consensus, which makes it the most comprehensive global standard on hazardous wastes. ISO 14001 is the Global standard for layout and implementing a hazardous waste management system

ISO/IEC 17025 General requirements for the competence of testing and Calibration labs is your main ISO standard used by testing and calibration laboratories. In most nations, ISO/IEC 17025 is the standard for which many labs need to maintain certification to be deemed technically competent. Oftentimes, providers and regulatory authorities won’t accept test or calibration results from a laboratory that isn’t accredited.

ISO/IEC 27001 is an international standard on how to handle Information safety. The standard was originally published together by the International Organization for Standardization (ISO) and the International Electrotechnical Commission (IEC) in 2005 [1] and then revised in 2013. [2] It details requirements for establishing, implementing, maintaining, and constantly improving an information security management system (ISMS) — the goal of which is to help organizations make the information resources they hold more secure. [3] A European upgrade of the standard was published in 2017. [4] Organizations that meet the standard’s needs can choose to be certified by an accredited certification body after successful completion of an audit.

ISO 45001, a Globally recognized International Standard Organization (ISO) standard for occupational health and safety management system, was established to address issues involving occupational health. The International Standard Organization, which will be a subdivision of the US National Committee for Standards is a not-for-profit organization that sets quality standards for products and services. An organization that has achieved the maximum status of “IEC 60 Annex 1” is an ISO member.