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

ISO 13485 Certification is for Quality control systems for medical instruments is an International Organization for Standardization, whose goal is to establish quality standards for pharmaceutical, biotechnological and generic drug products. The primary goal of ISO is to establish quality standards for drugs, generic drugs, and surgical materials and equipment that are used by health care and industrial industries in the production of medications, devices, and equipment. The organization sets quality objectives, quality control measures, quality management systems, performance data specifications, and labeling or packaging needs. This global standard has been accepted by different governments worldwide. As of the writing of this article, ISO has 27 member countries and is expanding rapidly in every area of pharmaceuticals business.

 ISO 14001 is the international Standard for creating and implementing a hazardous waste management system. ISO 14001 was established in 1996 to help facilitate the compliance of resources of hazardous wastes. Its objective is to establish a uniform system of engineering principles and guidelines necessary for handling such wastes. The standard is continuously updated through consensus, making it the most comprehensive international standard on hazardous wastes. ISO 14001 is the Global standard for layout and implementing a hazardous waste management program

 ISO/IEC 17025 General requirements for the competence of testing And calibration labs is the main ISO standard used by testing and calibration labs. In most countries, ISO/IEC 17025 is the norm for which most labs must maintain certification so as to be deemed legally capable. In many cases, suppliers and regulatory authorities won’t accept test or calibration results from a laboratory that is not accredited.

ISO/IEC 27001 is an Global standard on the best way to manage information security. The standard was initially published together by the International Organization for Standardization (ISO) and the International Electrotechnical Commission (IEC) at 2005[1] and then revised in 2013. [two ] 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 assets they hold more protected. [3] A European update of this standard was printed in 2017. [4] Organizations which meet the standard’s requirements can choose to be certified by an accredited certification body following successful completion of an audit.

ISO/IEC 27001 is a Global standard about the best way best to manage information security. The standard was initially 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 continually enhancing an information security management system (ISMS) — the aim of which is to help organizations make the data assets they hold more secure. [3] A European update of the standard was printed in 2017. [4] Organizations that meet the standard’s needs can opt to be certified by an accredited certification body after successful completion of an audit.

 ISO 45001, an Globally recognized International Standard Organization (ISO) standard For occupational health and safety management systems, was established to Address problems regarding occupational health. The International Standard Organization, that is a subdivision of the US National Committee for Standards Isn’t 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.