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The ISO 9000 family addresses various aspects of quality management and contains some of ISO's best known standards. The values provide guidance and tools for companies and organizations who want to ensure that their products and services constantly meet customer's necessities, and that quality is consistently improved.
This will give you the most valuable quality management system that will work for your business. It will provide a system that can be constantly monitored and improved upon by your internal team. In addition, an external assessor will bring in expertise and best practice from a wider industry observation. This will help to ensure that when the audit is done, your management systems comply with the necessities of ISO 9001:2008 Certification.
The ISO 9001 standard covers every part of your business management systems. It is therefore very important to appoint an assessor who has the experience to implement ISO 9001:2008 certification across all areas of your organization.
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ISO 9001:2008 sets out the criteria for a quality management system and is the only standard in the family that can be certified to (although this is not a requirement). It can be used by any organization, big large, huge or small, in spite of its field of activity. In fact ISO 9001:2008 is implemented by over one million companies and organizations in over 170 countries.
The appraiser can be appointed internally from senior management with the appropriate authority and expertise, or externally from an accredited certification body.
CE marking is a process that applies to a large variety of products and whose manufacturers located in the EU or importers of goods into the EU must comply it. The CE mark is affixed to the product as the final stage of this process and is efficiently a statement from the manufacturer that the process has been effectively completed and that the product meets the necessary requirements of the relevant CE marking directive.
The letters 'CE' appear on many products that are traded on the single market ie theEuropean Economic Area (EEA).
The CE marking is required for many products. It:
When the manufacturer of a machine puts the CE marking, it engage himself and guarantee, that he makes all the tests, assessments and evaluation on the product to conform all the requirements of ALL the directives that applies to its product.
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The RoHS directive aims to restrict certain dangerous substances generally used in electronic and electronic equipment. Any RoHS compliant component is tested for the presence of Lead (Pb), Cadmium (Cd), Mercury (Hg), Hexavalent chromium (Hex-Cr), Polybrominated biphenyls (PBB), and Polybrominateddiphenyl ethers (PBDE). For Cadmium and Hexavalent chromium, there must be less than 0.01% of the substance by weight at raw homogeneous materials level. For Lead, PBB, and PBDE, there must be no more than 0.1% of the material, when calculated by weight at raw homogeneous materials. Any RoHS compliant component must have 100 ppm or less of mercury and the mercury must not have been purposely added to the component. In the EU, some military and medical equipment are exempt from RoHS compliance.
Trooz Certification does more than simply help our customers comply, we give them a competitive advantage by partnering with them every step of the way to establish a detailed product file upon application that contains:
All compliance documents are subject to review and sample are required for RoHS 6-substance verification and testing of homogeneous materials. In addition, manufacturer site audits and observation for process management control will be implemented and executed to ensure compliance.
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There has never been a better time to adopt the OHSAS 18001 Standard as the foundation for your Occupational Health and Safety Management System (OHSAS). OHSAS is an internationally acknowledged occupational health and safety management system standard. It was published in July 2007, prevailing OHSAS 18001:1999, and is intended to deal with occupational health and safety rather than product safety.
First of all, the Health and Safety need of your staff and visitors should be evaluated. After that identify the limitations of your Health and Safety system and file your procedure for meeting the requirement of OHSAS 18001:2007. Make sure that these procedures will be fully implemented, then audit and review them. After system developed, internal audits are needed to ensure the system continues to be effective. Always bear in mind the requirement to conform to statutory necessities.
Organizations certified to the OHSAS 18001:2007 Standard report a range of benefits, including:
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