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

 ISO 13485 Certification is for Quality management systems for medical devices is an International Organization for Standardization, whose purpose would be to establish quality criteria for pharmaceutical, biotechnological and generic drug products. The main goal of ISO is to set quality criteria for drugs, generic drugs, and surgical materials and equipment that are used by healthcare and industrial industries in the creation of medicines, devices, and equipment. 

The company sets quality objectives, quality control measures, quality control systems, performance data specifications, and labeling or packaging needs. This global standard has been accepted by various governments worldwide. As of the writing of this article, ISO has 27 member states and is growing rapidly in every area of the biotech business.

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 countries, ISO/IEC 17025 is the norm for which many labs need to maintain certification to be deemed technically capable. In many cases, suppliers and regulatory authorities will not accept test or calibration results from a laboratory that isn’t accredited.

The International Standard Organization (ISO) is the sole authority for establishing quality parameters for goods. It sets the superior specifications used to determine what can and can’t be sold in the market. If a food or drink company wants to sell its goods in any country around the world, they have to be licensed to do so by the ISO. 

If you’re a producer who wants to market food items or beverages outside of your country, you must comply with each of the ISO 22000 regulations. Not doing so can lead to significant fines, penalties, and reduction of your business.

 ISO/IEC 27001 is an international standard on how to handle Information security. The standard was originally published jointly 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 goal of which is to help organizations create the data resources they hold more protected. [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 following successful completion of an audit.

ISO 45001, a Globally recognized International Standard Organization (ISO) standard for occupational health and safety management systems, was created to tackle problems regarding occupational health. The International Standard Organization, which is 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 standing of”IEC 60 Annex 1″ is an ISO member.