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RoHS Certification In Manipur

QbDelhi is one of the leading and fast rising certification bodies in Manipur with focus on customer pleasure through valuable services in Manipur. QbDelhi certification body involving of highly qualified professionals proposing the latest in systems certification and promoting quality concepts. QbDelhi is originally registered in India, and can provide certificate accredited from Dubai Accreditation Department (DAC), JASANZ, UKAS, SCOTLAND Accreditation Forum for ISO 9001:2008 Standard, ISO 14001:2004 Environment Management System Standard, ISO/IEC 27001 Information Security Management System (ISMS), ISO 22000:2005/HACCP Food Safety Management System. We issues guarantee expert level of work and approach. QbDelhi is also dependent certification and Consultancy firm for other international standards like ISO 14001, OHSAS 18001 Occupational Health and Safety Management, ISO 27001 Information Security Management System ANDISO 22000. We offerISO certificate services in Manipur.

We arrange for ISO certificate services in various parts of Manipur etc. Any company and organization can follow ISO authorization to set up an effective certification process, which is very essential for development of a company or organization. We hope a company definitely understands the profits and process for obtaining the ISO certification. We have the right training courses, services and resources. We offer packages that can be modified to your business to startup in Manipur.

QbDelhi is bound up to be a leader in provided thatvaluable, independent and impartial Management System Certificate Services in Manipur, maintaining customer focus during all phases of preparation and service provision with emphasis on continual development and enhance the service the excellence of being believable for worldwide recognition, customer faithfulness and capable of being sustained performance. QbDelhi Certificates is committed to administer non-discriminatory policy in all the services delivered and demonstrate independence, integrity and Impartiality by planned and effective management of struggle of interest during all phases of certification process service distribution in Manipur.

QbDelhi is an Independent Assessment and Certification offering valuable services in the field of: ISO 9001, ISO 14001, ISO 22000& CE Mark Certification in Manipur.

ISO 9001:2008 Certification in Manipur

The purpose of ISO 9001:2008 is to facilitate international trade by provided that a single standard that is recognized and valued globally. It is a basic standard and is applicable to organizations in all areas of work. Some of the areas are manufacturing, processing, servicing, printing, electronics, forestry, steel, computing, financial services, legal services, accounting, trucking, banking, retailing, and so on. We provide ISO 9001 certificate services in Manipur.

ISO 14001:2004 Environmental management systems Certificate In Manipur

An Environmental Management System is a framework, which can be integrated with standing business processes to effectively identify measure, manage and control environmental effects and therefore environmental risks. An Environmental Management System also establishes the means for refining performance and moving towards environmental sustainability through best practice such as ISO14001 in Manipur.

ISO 18001:2007 Certification In Manipur

An occupational health and safety management system will place the basic necessities for a safe and secure environment. This will make sure that your business practices the right methods and standards to offer your employees a safe and protected time at work. If you have a business that is in the manufacturing, operating etc. side of works, it would make logic to have a certification that make sure the safety of all your employees. There are a lot of occupational hazards that could be in place and you need to safeguard your employees from each one of them. We provide OHSAS 18001 certificates in Manipur.

ISO 27001:2005 Information Security Management Systems Certification In Manipur

Information is a valuable asset that can make or pause your business. When properly managed it allows you to operate with confidence. Information security management gives you the independence to develop, invent and broaden your customer-base in the information that all your confidential information will remain that way.

The ISO 27001 standard was issued in October 2005. It is the specification for ISMS, an Information Security Management System. BS7799 itself was a long standing standard, first published in the nineties as a code of practice. As this matured, a second part emerged to cover management systems. Today in excess of a thousand certifications are in place, in Manipur.

TS 16949 Automotive Industry Standard Certification In Manipur


The ISO/TS16949 is an ISO technical specification targeting to the development of a quality management system that provides for continual improvement, emphasizing faultstoppage and the reduction of variant and waste in the supply chain. It is built on the ISO 9001 and the first edition was published in March 2002 as ISO/TS 16949:2002.

It was organized by the International Automotive Task Force (IATF) and the "Technical Committee" of ISO. It harmonizes the country-specific regulations of Quality Management Systems.

About 30 percent of the more than 100 existing automobile manufacturers affiliate the requirements of the norm but specifically the large Asian manufacturers have differentiated, own requirements for the quality management systems of their corporate assembly and their suppliers.

TS16949 put on to the design/development, manufacture and, when relevant, installation and servicing of automotive-related products.

ISO/IEC 17025 Certification In Manipur

ISO/IEC 17025 General necessities for the competence of testing and calibration research laboratory are the main ISO standard used by testing and calibration laboratories. Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by the International Organization for Standardization in 1999. ISO/IEC 17025 is more precise in requirements for competence. And it applies straight to those organizations that produce testing and calibration results. Since its initial announcement, a second announcement was made in 2005 after it was agreed that it needed to have its quality system words more closely aligned with the 2000 version of ISO 9001.

The ISO/IEC 17025 standard itself includes five elements that are Scope, Normative References, Terms and Definitions, Technical Requirements and Management Requirements. The two main sections in ISO/IEC 17025 are Management Requirements and Technical Requirements. Management requirements are primarily related to the operation and effectiveness of the quality management system within the research laboratory. Technical requirements includefactors which determine the exactness and reliability of the tests and calibrations performed in research laboratory.

Research laboratory use ISO/IEC 17025 to implement a quality system aimed at improving their skill to consistently produce valid results. It is also the basis for accreditation from accreditation bodies. Since the standard is about competence, accreditation is basically formal acknowledgement of a demonstration of that competence. A precondition for a research laboratory to become accredited is to have a documented quality management system. The usual contents of the quality manual follow the outline of the ISO/IEC 17025 standard.

ISO 13485:2012 Medical Device Quality Management Standard Certification In Manipur

ISO 13485 is an International Organization for Standardization (ISO) standard, published in 2003, that signifies the requirements for a comprehensive quality management system for the design and production of medical devices. This standard replaces earlier documents such as EN 46001 and EN 46002 (both 1997), the ISO 13485 published in 1996 and ISO 13488 (also 1996)

Though it is tailored to the industry's quality system prospects and regulatory requirements, an organization does not need to be actively manufacturing medical devices or their components to search for certification to this standard, in against of the automotive sector's ISO/TS 16949, where solitary firms with an active request for quotation, or on the bid list, of an International Automotive Task Force supply chain manufacturer can search for registration.

While it remains a stand-alone document, ISO 13485 is generally consistent with ISO 9001. A principal difference, however, is that ISO 9001 requires the organization to demonstrate constant development, whereas ISO 13485 requires only that the certified organization demonstrate the quality system is effectually executed and maintained. Additionally, the ISO 9001 requirements regarding customer gratification are absent from the medical device standard.

TOTAL QUALITY MANAGEMENT (TQM) In Manipur

Total quality management (TQM) consists of organization-wide efforts to install and make everlasting a environment in which an organization continuously increases its ability to deliver high-quality products and services to customers. While there is no widely agreed-upon approach, TQM efforts typically draw heavily on the previously established tools and techniques of quality control. TQM enjoyed prevalent attention during the late 1980s and early 1990s before being overshadowed by ISO 9000, Lean manufacturing, and Six Sigma.

GMP Certification In Manipur

Good manufacturing practices (GMP) are the practices required in order to conform to guidelines suggested by agencies that control endorsement and licensing for production and sale of food, drug foodstuffs, and active pharmacological products. These guidelines make available minimum requirements that a pharmaceutical or a food product manufacturer must meet to assure that the products are of high quality and do not pose any danger to the consumer or public.

Good manufacturing practices, along with good research laboratory practices and good clinical practices, are managed by regulatory agencies in the United States, Canada, Europe, China, in addition to other countries.

RoHS (Restriction of Hazardous Substances) Compliance Certification In Manipur

The Restriction of Hazardous Substances Directive 2002/95/EC, RoHS, short for Directive on the restriction of the use of assured hazardous substances in electrical and electronic equipment, was accepted in February 2003 by the European Union.
The RoHS directive took result on 1 July 2006, and is required to be forced and become law in each member state. This directive controls the use of six hazardous materials in the manufacture of various types of electronic and electrical equipment. It is narrowly linked with the Waste Electrical and Electronic Equipment Directive (WEEE) 2002/96/EC which sets collection, recycling and recovery goals for electrical goods and is part of a legislative inventiveness to resolve the problem of vast amounts of toxic e-waste.

NABH Certification In Manipur

Organizations like the Quality Council of India (QCI) and its National Accreditation Board for Hospitals and Healthcare providers have designed athorough healthcare standard for hospitals and healthcare workers. This standard consists of stringent 600 plus objective fundamentals for the hospital to achieve in order to get the NABH accreditation. These standards are separated between patient centered standards and organization centered standards.

To comply with these standard fundamentals, the hospital will need to have a process-driven approach in all aspects of hospital activities – from registration, admission, pre-surgery and post-surgery protocols, release from the hospital to follow-up with the hospital after release. Not only the clinical features but the governance features are to process driven based on clear and transparent policies and protocols. In a nutshell NABH aims at streamlining the whole operations of a hospital.

NABH is equal to JCI and other International standards plus HAS: Haute Authority de Santé, Australian Council on Healthcare Standards, the Japan Council for Quality in Health Care, and the National Committee for Quality Assurance in the United States.

Medication Errors can be avoided at the point of care within the hospitals; medicament points like OPs and drug dispense sing points like chemist's and nursing stations by the use of reliable and updated drug information, e.g. Meddle.

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