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ISO 9001 Certification Jharkhand India
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.
Benefits of ISO 9001 Quality Management System Certification from Trooz Certification in Jharkhand India
- Motivate and engage staff with more efficient internal processes
- More efficient ways of working will save resources, money and time.
- Enlarge business opportunities by signifying compliance
- Improved operational performance will increase profits and cut errors
- Allows you to become a more steady challenger in your marketplace
- Win more high value customers with improved customer service
- Better quality controlling helps you meet customer needs
BENEFITS OF ISO 9001
- Reduced operating costs. Recurrent improvement of processes and resulting operational efficiencies mean money saved.
- Proven business credentials. Independent verification against a worldwide recognized industry standard speaks volumes.
- Skill to win more business. Procurement specification often require certification as a condition to supply, so certification opens doors.
- Improved stakeholder relationships. Improve the perception of your organization with supplier, staff and customers.
- Legal compliance. Understand howstatutoryand regulatoryrequirements impact your organization and its customers.
- Customer satisfaction. Deliver products that constantly meet customer necessitie.
- Improved risk management. Greater traceability and consistency of products and services means problems are easy to avoid and rectify.
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
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:
- shows that the manufacturers has checked that these products meet EU safety, health or environmental necessitie
- allows the free movement of products within the European market
- is an indicator of a product’s compliance with EU regulation
Characteristics of CE marking
- The CE marking has to be affixed by the manufacturer or its official representative in the European Union according to its legal format visibly, legibly and indelibly to the product.
- When a manufacturer puts the CE marking on a products this implies that he complies to all the Essential Health and safety requirements from all the directives that applies to its product.
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.
- CE marking has been introduced by the COUNCIL DIRECTIVE 93/68/EEC of 22 July 1993 amending Directives 87/404/EEC (simple pressure vessels), 88/378/EEC (safety of toys), 89/106/EEC (construction products), 89/336/EEC (electromagnetic compatibility), 89/392/EEC (machinery), 89/686/EEC (personal protective equipment), 90/384/EEC (non-automatic weighing instruments), 90/385/EEC (active implantable medicinal devices), 90/396/EEC (appliances burning gaseous fuels), 91/263/EEC (telecommunications terminal equipment), 92/42/EEC (new hot-water boilers fired with liquid or gaseous fuels) and 73/23/EEC (electrical equipment designed for use within certain voltage limits)
- The size of the CE marking must be at least 5 mm, if enlarged its proportions have to be kept.
- If a directive requires the participation of a Notified Body in the conformity assessment procedure, its identification number has to be put behind the CE logo. This is done under the responsibility of the Notified Body.
CE marking applies to products, ranging from electrical equipment to toys and from civil explosives to medical devices. The full list of these product categories is below:
- appliances burning gaseous fuels
- cableway installations designed to carry persons
- eco-design of energy related products
- electromagnetic compatibility
- active implantable medical devices
- equipment and protective systems intended for use in potentially explosive atmospheres
- explosives for civil uses
- hot-water boilers
- household refrigerators and freezers
- in vitro diagnostic medical devices
- pyrotechnics
- radio and telecommunications terminal equipment
- lifts
- low voltage
- machinery
- measuring instruments
- active implantable medical devices
- medical devices
- noise emission in the environment
- non-automatic weighing instruments
- personal protective equipment
- pressure equipment
- recreational craft
- safety of toys
- simple pressure vessels
The CE marking is not essential for items:-
- Chemicals
- cosmetics and foodstuffs
- pharmaceuticals
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ROHS CERTIFICATION Jharkhand India
RoHS Compliance
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.
RoHS Certification Services
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:
- Test report
- Materials declarations from the suppliers of material and/or components
- Declarations of Conformity (DoC)
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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OHSAS 18001:2007
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.
IMPLEMENTATION OF OHSAS 18001
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.
The benefits of OHSAS 18001:2007 Standard
Organizations certified to the OHSAS 18001:2007 Standard report a range of benefits, including:
- Missing working days are reduced
- A more disciplined approach to safety
- Less workplace accidents
- Improved employee motivation, retention and satisfaction
- Medical claims are less
- Acknowledged by insurers and regulators
- Less time & money spent on investigation and paperwork accident
- Legal cost is reduced
Key areas that will be assessed by OHSAS 18001:2007 certification
- Management systems in place
- Communication of safety management systems
- Planning and risk assessment
- Staff training and awareness
- Monitoring and continual improvement
- Response to emergency situations
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| ISO Certification Company |
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| New Delhi - 110018 (India) |
| Contact: Mr. Vinay #91-9868301527 |
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