ISO 9001:2008 Quality management systems – Requirements is intended for use in any organization which designs, develops, manufactures, installs and/or services any product or provides any form of service. It provides a number of requirements which an organization needs to fulfill if it is to achieve customer satisfaction through consistent products and services which meet customer expectations. It includes a requirement for the continual (i.e. planned) improvement of the Quality Management System
Archive for September 20th, 2009
ISO 9001 : 2008 Standard – requirements and implementation guide – how to get iso 9001 certificte for your company
September 20th, 2009 
ISO Certification Consultants 
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2 Comments »OHSAS 18001 DOCUMENTATION,IMPLEMENTATION & CERTIFICATION :- WHITE PAPER
September 20th, 2009 ISO Certification Consultants All organizations, regardless of their size or complexity are faced with the challenge of implementing an occupational safety and health (OH&S) management system that would prevent injuries and ill health to persons that are working under the control of the organization (contractors, employees). The Occupation Health and Safety Assessment Series (OHSAS) 18001 standard has been successfully adopted by many organizations to manage their (OH&S) hazards and risks.
OHSAS 18001 is a standard that specifies how an occupational safety and health management system should be designed. The standard provides a framework for organizations, regardless of their complexity or size, to holistically manage their occupational safety and health risks though a simple PLAN-DO-CHECK-ACT system of management. This management model is found in other management system standards such as ISO 9001 and ISO 14001. Therefore organizations have found it convenient to integrate OHSAS 18001 into their existing ISO 9001 and/or ISO 14001 systems.
Posted in HOW TO ACHIEVE OHSAS 18001 CERTIFIACATION, OHSAS 18001, OHSAS 18001 CERTIFICATION, OHSAS 18001 CONSULTANTS INDIA MUMBAI SAUDI ARABIA UAE DUBAI, OHSAS 18001 CONSULTING, OHSAS 18001 documentation, OHSAS 18001 IMPLEMENTATION, OHSAS 18001 INTRODUCTION, OHSAS 18001:2007 DOCUMENTATION, REQUIREMENTS OF OHSAS 18001 STNDARD Tags: HOW TO ACHIEVE OHSAS 18001 CERTIFIACATION, OHSAS 18001, OHSAS 18001 CERTIFICATION, OHSAS 18001 CONSULTANTS INDIA MUMBAI SAUDI ARABIA UAE DUBAI, OHSAS 18001 CONSULTING, OHSAS 18001 IMPLEMENTATION, OHSAS 18001 INTRODUCTION, OHSAS 18001:2007 DOCUMENTATION, REQUIREMENTS OF OHSAS 18001 STNDARD 1 Comment »Demonstrate your ability to supply medical devices through Quality Management System for Medical Devices – ISO 13485
September 20th, 2009 ISO Certification Consultants ISO 13485 is the quality management system standard for medical devices. This standard applies the ISO 9001:2008 process approach to quality, and replaces ISO 13485:1996 and ISO 13488:1996.
ISO 13485:2003 provides an effective base model for compliance with the EU CE marking Medical Devices Directives requirements. ISO 13485:2003 is also considered to be fully compatible with the FDA QSR.
ISO 13485 is an international standard, recognized throughout the world for establishing a business management system specific to the medical device industry. ISO 13485 is applicable to organizations that manufacture private label medical devices, in vitro diagnostic medical devices, and medical components.
Writing an Environmental Policy
September 20th, 2009 ISO Certification Consultants Writing an Environmental Policy
Looking for help on writing an environmental policy? The guide gives an introduction to why you should have one, the associated benefits and how to write one for your own organisation.
