Iso 9000 pdf free download

Iso Presentation. Introduction to ISO The iso series ppt. Project Report on ISO. Concept of ISO. Related Books Free with a 30 day trial from Scribd. Related Audiobooks Free with a 30 day trial from Scribd. Elizabeth Howell. AnAgha ViNod. Sai Sumanjali Yarra , Research Scholar. Dr-Gourav Bharat.

Smita rao. Sharmishtha Hada , Lecturer at Truba college of science and technology, bhopal at Truba college of science and technology, bhopal. Show More. Views Total views. Actions Shares. No notes for slide. ISO pdf 1.

Pharma Q. In fact, companies not ISO-certified would find it difficult to do business, given that certification is a basic requirement of would-be customers.

This means that ISO is more particular about how a company conducts its processes, and not what products it ships or level of product quality it has.

The ISO, being processoriented, can be applied to virtually any industry worldwide, and is certainly widely embraced in the semiconductor industry. ISO and ISO had been dropped, so companies who are certified to any of these two standards only should be re-certified to the ISO Companies certified to the ISO need to update their quality systems to the ISO requirements for future recertification. With the exception of the electrical and electronic engineering industries which are covered by International Electrotechnical Commission - IEC , the ISO is responsible for the promotion and development of international standards and related activities, including conformity assessments such as testing, inspection, laboratory accreditation, certification and quality assessments.

One very important aspect of the standards is that they were very generic in nature and ingenuity is required while interpreting the standards' applicability to the industry or firm in question. This is the most comprehensive high standard with 20 clauses. This standard has 18 clauses sarte. Requires conformity with 12 clauses sarte. This is because the number of companies desirous of getting an ISO series registration is ever increasing.

In addition to the registrars, the number of people providing ISO related services such as consultancy on ISO implementation and lead assessor courses is also showing exponential growth. Apex industry associations such as the CII Confederation of Indian Industry have also started providing services such as the lead assessor course.

The best strategy to adopt when embarking on the road to ISO registration is to adopt a simple model: design a quality assurance model from bottom up to ensure that what is done is indeed what is documented. Most auditors, while doing third party audits for registration, like to follow the "show me mapping" process.

The process should begin with a familiarisation with the standard, followed by an assessment of the current quality assurance system with a special focus on how it addresses the ISO requirements. Thereafter, corrective actions to remove the gaps should be initiated and continuous monitoring via internal quality audits should take place to prevent the degradation of the systems' entropy to a higher level. It is advisable to have the assistance of a consultant to guide the implementation efforts.

The registrars, after conducting the audit, send their recommendations to the accrediting body, which gives the certification. After certification, periodic "unannounced" audits are conducted to ensure that the unit is complying with the requirements of the standard.

Incidentally, it makes good sense to decentralise registration efforts both from the point of view of acquiring as well as retaining certification. The designed Quality Assurance system should: - suit the unit's need, not be restrictive to the point of being impractical be continuously upgraded.

Indeed the implicit driving force behind the registration process should be the formulation of a well throughout, effective system designed to bring about improved performance. In fact, it is only a base line model for quality assurance, which can and should be upgraded continuously. It represents a documented system for quality assurance and the real benefit besides improved quality it offers is that it raises the confidence of the third party dealing with the registered unit.

There is indeed a facelift in the organisation's corporate image and not surprisingly, an advertising campaign follows the registration. There are other technical benefits of registration as well. Since the adoption of the Resolution of May 7, , concerning a new approach towards technical 5.

With over 1. It also acts as a tool to streamline their processes and make them more efficient at what they do. ISO E 0. The earlier versions of ISO were quite prescriptive, with many requirements for documented procedures and records.

In the and editions, we focused more on managing processes, and less on documentation. We have achieved this by combining the process approach with risk-based thinking, and employing the Plan-Do-Check-Act cycle at all levels in the organization. The new version also provides a solid base for sector-quality standards automotive, aerospace, medical industries, etc. Technology is driving increased expectations from customers and businesses. Barriers to trade have dropped due to lower tariffs, but also because of strategic instruments like International Standards.

We are seeing a trend towards more complex global supply chains that demand integrated action. So organizations need to perform in new ways, and our quality management standards need to keep up with these expectations. I am confident that the edition of ISO can help them achieve this. I thank the experts for their hard effort. ISO replaces previous editions and certification bodies will have up to three years to migrate certificates to the new version.