Ideal Quality Certifications

Kandivali East, Mumbai, Maharashtra

ISO 9001:2015 certification is acclaimed for being a management tool worldwide. With eight management principles as its base, this certification deals with the fundamentals of quality management of products in any sector, regardless of its type and size. It is claimed to be the sole standard of the 9000 family against which an organization can be certified. Innumerable organizations in India adopt a quality management system as a strategic growth policy. Its benefits include the enhancement in customer satisfaction by meeting their requirement, effective resource management, improvement in procedures, and others. You can confirm the declaration of your product/service by turning to Ideal Quality Certifications.

Main Requirements of the ISO 9001 Standard :Clause 1. ScopeClause 2. Normative ReferencesClause3. Terms and DefinitionsClause 2. Normative References Clause3. Terms and Definitions Clause 4. Quality Management System (2 Elements) Clause 5. Management Responsibility (6 Elements) Clause 6. Resource management (4 Elements) Clause 7. Product / Service Realization (6 Elements) Clause 8. Measurement, Analysis and Improvement (5 Elements)Clause 2. Normative References Clause3. Terms and Definitions Clause 4. Quality Management System (2 Elements) Clause 5. Management Responsibility (6 Elements) Clause 6. Resource management (4 Elements) Clause 7. Product / Service Realization (6 Elements) Clause 8. Measurement, Analysis and Improvement (5 Elements)Meet your needs and expectationsComply with applicable regulations
The requirements cover a wide range of topics, including your supplier's top management commitment to quality, its customer focus, adequacy of its resources, employee competence, process management (for production, service delivery and relevant administrative and support processes), quality planning, product design, review of incoming orders, purchasing, monitoring and measurement of its processes and products, calibration of measuring equipment, processes to resolve customer complaints, corrective/preventive actions and a requirement to drive continual improvement of the QMS. Last but not least, there is a requirement for your supplier to monitor customer perceptions about the quality of the goods and services it provides. ISO 9001 does not specify requirements for the goods or services you are purchasing. That is up to you to define, by making clear your own needs and expectations for the product. You might, for example, refer to product specifications, drawings, National or International product standards, supplier’s catalogues or other documents as appropriate.

What does "Conformity to ISO 9001 mean? :This means that your supplier has established a systematic approach to quality management, and is managing its business to ensure that your needs are clearly understood, agreed and fulfilled. A statement of conformity to ISO 9001 should not, however, be considered as a substitute for a declaration or statement of product conformity.

How does ISO 9001 help you in selecting a supplier? :ISO 9001 provides some requirements for the purchasing process that include you as the customer. These requirements address the following topics - Requirements regarding the purchasing information that should be provided so that suppliers clearly understand their customers' needs. the ways in which supplied products can be verified as meeting the requirements of the customer.
Note that whenever ISO 9001 refers to “products? this also includes intangible products like services, or software. You have an important role to play, by specifying to your supplier what you actually want. You may need to consult with your own internal technical staff (the actual users) in this process. If you don’t do this, you might find that you receive a product that meets all your stated requirements and the applicable regulatory requirements, but which is absolutely wrong for your intended application. So, first of all, you should concentrate on specifying your needs related to the intended use of the product.

To help in this task you may consider the following :

• What is the specific product (goods or service) you are buying?
• What impact does this product have on your own business?
• What are the risks to your business if you experience problems with this product?
• How can you be sure that the product you receive will actually meet your requirements?
• What do you know about the reputation and historical performance of your supplier?
• What level of confidence do you need in your supplier’s ability to provide you with conforming product on a consistent basis?
• If you decide that conformity to ISO 9001 is important, (based on your assessment of the risks associated with the goods and services you are buying) how can you be sure that your supplier does have a QMS that meets ISO 9001 requirements?
• Are the goods and services you require covered by your supplier’s QMS? (You may need to ask for a copy of your supplier’s actual certificate or declaration of conformity to find this out!)

How can you have confidence that your supplier meets ISO 9001? :

• There are various ways in which your supplier can claim that its QMS meets the requirements of ISO 9001. These include :
• Supplier’s declaration of conformity? A declaration by your supplier itself affirming that its QMS meets ISO 9001 requirements, usually supported by legally-binding signatures. This declaration can be based on your supplier’s internal audit system, or on second party or third party audits;
• Second party assessment: your supplier has been assessed directly by its customer (for example by you, or by another customer, whose reputation you respect) to check if its QMS meets ISO 9001 requirements and your own requirements - sometimes used in contractual “business-to-business?transactions;
• Third party assessment: (often referred to as certification or registration): your supplier hires an impartial third party (a Certification Body, or “Registrar? to conduct an assessment to verify conformity to ISO 9001 requirements. This third party then issues a certificate to your supplier describing the scope of its QMS, and confirming that it conforms to ISO 9001
• Additional confidence may be derived from the fact that some Certification Bodies (“Registrars? are accredited by nationally or internationally recognized Accreditation Bodies, who verify the certification body’s independence and competence to carry out the certification process. Many accreditation bodies have multi-lateral arrangements under the umbrella of the IAF (International Accreditation Forum) to promote worldwide mutual recognitions in support of WTO (World Trade Organization) free trade principles.

Can suppliers claim that their goods or services meet ISO 9001?No. The reference to ISO 9001 indicates that the supplier has a quality management system that meets the requirements of ISO 9001. As mentioned earlier, this should provide you with confidence in your supplier’s ability to provide consistent, conforming goods or services. ISO 9001 requires your supplier to monitor the levels of satisfaction of its customers (this includes you!), and to feed back this information in order to improve the effectiveness of its QMS.

Released in 2001, ROHS is an abbreviation for Restriction of Hazardous Substance directive. As per this certification, all electronic items and appliances require to be manufactured without the usage of six hazardous materials like lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls, and polybrominated diphenyl. Since many electronic items are disposed on a huge scale, they cause great damage to environment. Every electronic item having the authentic mark of ROHS certificate denotes that a particular item doesn’t comprise or exceed the standardized levels of hazardous substances. Manufacturers of electronic items and electrical appliances can approach Ideal Quality Certifications and receive the ROHS certificate for their products.

What is RoHS? :RoHS is known as the Restriction of Hazardous Substances Directive. It restricts the usage of six specific hazardous substances in the manufacture of certain electronic products.

When was RoHS released? :RoHS was initially released in 2003.

Who released RoHS? :RoHS was released by the European Union.

The Electrical and Electronic Equipment Act :This Directive bans placing on the EU market electrical and electronic equipment containing more than agreed levels of lead, cadmium, mercury, Hexavalent chromium, polybrominated biphenyl (PBB) and polybrominated diphenyl ether (PBDE) flame retardants.Product categories covered are household appliances (large & small), IT & telecommunications equipment, consumer equipment, lighting equipment, electrical / electronic tools, toys / sports equipment, medical devices, monitoring / control instruments and automatic dispensers.

A CE marking certification is a legally mandated conformity for all products and services that are regulated by the new approach directives, a series of European health safety, environmental, and consumer protection laws. The CE marking is mandatory as it describes that the certain product/service is manufactured/rendered in compliance with general industrial safety standards. The CE marking is essential for various products like toys, machinery, electronic items, protection equipment, pressure equipment, medical devices, boilers, and much more. Ideal Quality Certifications encompasses all industry standards and our R&D professionals thoroughly inspect the products prior to giving it the CE certification.

General principles of the CE marking :

• The CE marking shall be affixed only by the manufacturer or his authorised representative.
• The CE marking shall be affixed only to products to which its affixing is provided for by specific Community harmonisation legislation, and shall not be affixed to any other product.
• By affixing or having affixed the CE marking, the manufacturer indicates that he takes responsibility for the conformity of the product with all applicable requirements set out in the relevant Community harmonisation legislation providing for its affixing.
• The CE marking shall be the only marking which attests the conformity of the product with the applicable requirements of the relevant Community harmonisation legislation providing for its affixing.
• The affixing to a product of markings, signs or inscriptions which are likely to mislead third parties regarding the meaning or form of the CE marking shall be prohibited. Any other marking may be affixed to the product provided that the visibility, legibility and meaning of the CE marking is not thereby impaired.
• Member States shall ensure the correct implementation of the regime governing the CE marking and take appropriate action in the event of improper use of the marking. Member States shall also provide for penalties for infringements, which may include criminal sanctions for serious infringements. Those penalties shall be proportionate to the seriousness of the offence and constitute an effective deterrent against improper use.

How to achieve CE mark approval, CE testing and meet all CE mark requirements, for my product?:There are a series of steps outlined below for CE mark approval. Depending upon your product and the nature of the risks it presents - Determine if any directives apply to your product. If more than one applies you will have to comply with all of them. Determine the extent to which your product complies with the essential requirements for design and manufacturing in the applicable directive(s).Choose the conformity assessment procedure from the options (modules) called out by the directive for your product. There are several modules available for the Conformity Assessment Procedures as listed below :

• Module A - internal production control
• Module Aa - intervention of a Notified Body
• Module B - EC type-examination
• Module C - Conformity to type
• Module D - Production quality assurance
• Module E - Product quality assurance
• Module F - Product verification
• Module G - Unit verification
• Module H - Full quality assurance

The directives often use a series of questions about the nature of your product to classify the level of risk and refer to a chart called "Conformity Assessment Procedures". The chart includes all of the acceptable options available to a manufacturer to certify their product and affix the CE Marking.

Minimal Risk :Options for products with minimal risk include self certification where the manufacturer prepares a Declaration of Conformity and affixes the CE Marking to their own product.

Greater Risks :Many directives require products/systems with greater risks to be independently certified; this must be done by a "Notified Body". This is an organization that has been nominated by a Member Government and has been notified by the European Commission. Notified bodies serve as independent test labs and perform the steps called out by directives. They must have the necessary qualifications to meet the testing requirements set forth in the directives. Notified bodies may be a private sector organization or a government agency. Manufacturers may choose a notified body in any member state of the European Union.

A Notified Body is usually able to offer some of the services required :

• Product testing
• Type examination certificate issue
• Technical File and design dossier evaluation
• Surveillance of product and quality system
• Identification of standards

Commonly known as EMS, this certification defines the management requirements for all environmental management systems. This standard serves the purpose of saving the environment from different types of industrial hazards like preventing the fume emission and keeping an eye on all environmental protection measures. Its prime motive also adheres with saving the cost by making the resources more efficacious, optimizing the use of all available resources, increasing the cost by reducing the industrial waste, and much more.

Benefits of ISO 14001 :

• ISO 14001 drives protection of environment and help organizations :
• Reduce costs and increase profit through reduced waste and energy, reuse and recycle through 3R concept.
• Optimize use of resources (electrical, water and materials).
• Increase competitiveness.
• Reduce costs as a result of potential lower insurance rates.
• Environmentally responsible and commitment to environment protection.
• Cost saving through improved efficiency and productivity.
• Boost company’s public image.

How to use ISO 14001 :If you don’t already have an Environmental Management System (EMS), you can use this ISO 14001 standard to establish one. And once you’ve established your EMS, you can use it to manage the environmental aspects of your organization’s activities, products and services, and to improve its overall environmental performance. Environmental performance is all about how well you manage and control your environmental aspects and the impact they have on the environment.
You can also use this standard to demonstrate that you are doing everything you can to protect the environment and improve your environmental performance. You can demonstrate your organization’s commitment in several ways :

• You can simply announce to the world that your EMS complies with the ISO 14001 standard (if it actually does).
• You can ask your customers or other interested parties to confirm that your EMS complies with the ISO 14001 standard.
• You can ask an ISO 14001 registrar or external auditor to verify that your EMS complies with the ISO 14001 standard.

ISO 14001 expects organizations to comply with all of the requirements that make up the standard. No exceptions. According to ISO, every ISO 14001 requirement must be built into every EMS. However, the size and complexity of Environmental Management Systems vary quite a bit.
How far you go is up to you. The size and complexity of your EMS, the extent of your documentation, and the resources allocated to it will depend on many things. How you meet each of the ISO 14001 requirements, and to what extent, depends on many factors, including :

• The size of your organization
• The location of your organization.
• The scope of your organization’s EMS.
• The content of your environmental policy.
• The nature of your activities, products, and services.
• The environmental impact of your environmental aspects.
• The legal and other requirements that must be met.

Every company and organization has sensitive data that usually comprises the information about its resources and other private documents. Ideal Quality Certifications is engaged in rendering ISO 27001 ISM services to multiple companies. We are aided by a staff of professionals that are bifurcated into teams. They accordingly examine the possible risks and vulnerability of the potential risks and create a coherent suite of information of security controls. The benefits of ISO 27001 IMS include regular assessment, enhancement of security awareness, and much more.

ISO 27001 Information Security Management Certification ServicesAn Information Security Management System (ISMS) provides a systematic approach to managing sensitive information in order to protect it. It encompasses employees, processes and information systems.

• Systematically examines the organization’s information security risks, taking account of the threats, vulnerabilities and impacts;
• Designs and implements a coherent and comprehensive suite of information security controls and/or other forms of risk treatment (such as risk avoidance or risk transfer) to address those risks that it deems unacceptable; and
• Adopts an overarching management process to ensure that the information security controls continue to meet the organization’s information security needs on an ongoing basis.

ISO 27001 Consultant – Benefits :

• The provision of a for resolving security issues
• Independently verifies that your risks are properly identified, assessed and managed, while formalizing information security processes, procedures and documentation.
• Enhancement of client confidence and perception of your organisation
• Provides confidence that you have managed risk in your own security implementation
• Enhances security awareness within an organisation
• The regular assessment process helps you continually monitor and improve your ISMS.

How can Sai Quality Certification help to get ISO 27001 Consultant? :full-time trainers and consultants having huge international experience and exposure in ISO 27001:2005 ISMS certification, implementation and training.

TS 16949:2009 automotive certification was founded by the International Automotive Task Force. At the time of its establishment, the founding committee included renowned companies like BMW, Volkswagon, General Motors, Ford, Fiat, Daimler-Chrysler, Renault SA etc. Since the global automotive industry demands inimitable quality of the automobile, its design, engine, and spare parts, the manufacturers & suppliers in the automotive sector adhere to the regulations and industry standards for receiving TS 16949:2009 automotive certification.

ISO/TS 16949 Implementation Guide :Suppliers are required to transition to ISO/TS 16949 by December 14th 2006 or as specified by their customer. The weakest part of QS9000 was the implementation of the standard, both from a supplier and registrar's perspective.

How this document fills the need :This implementation guide gives us an opportunity to improve ISO/TS 16949 implementation based on lessons learned from QS9000 by :

• Defining what's new and different between QS9000 Third Edition and ISO/TS 16949
• Providing an explanation of the process approach
• Developing strategies for implementation
• Explaining pitfalls to avoid

Supporting documents for ISO/TS 16949 :

• Rules for Achieving Iatf Recognition :
  • This contains the requirements or “Rules for the automotive registration scheme for ISO/TS 16949 certification bodies?with regard to implementation including criteria for certification body recognition, certification body audit process, certification body auditor qualifications and, certificates. For certification bodies that are recognised by IATF for ISO/TS 16949 certification, these requirements are binding.

IATF Guidance to Iso/ts 16949 :This document is limited to providing assistance in the application of ISO/TS 16949. It is not intended as a requirement for certification and is for reference only. It supports the ISO/TS 16949, with examples, applications, practices or explanations. This guide is intended to apply to sites of organisations where production and/or service part specified by the customer are manufactured. It may also be applied to organisations throughout the automotive supply chain.

(QMS) Checklist Based On Process Audit Approach :This document is based on the content of ISO/TS 16949 and it is effective for the life of this standard. This checklist is to be used as a guide in auditing the requirements of ISO/TS 16949.

17025:2005 certification is offered by Ideal Quality Certifications. This program is essential for all laboratories that perform tests in different types of industries all over India.  The testing & calibration labs comply with industry standards in order to work with ISO 9000. ISO 17025 was developed to provide an identity to all labs that perform calibration and tests. Each decision is based on decisions that are accurate, verified, cost-effective, and semi-opinionated.

What is ISO 17025? :

• ISO 17025 was developed so that testing & calibration laboratories were recognized for their capabilities & areas of competence. All measurements and decisions should be based on accurate, repeatable, verifiable, cost effective, timely, and believable measurements, opinions, and recommendations. ISO 17025 helps assures this happens first time, every time, and on-time.
• Without these assurances, the data, opinion, and recommendations are immediately suspect, questionable, risky, and of greatly reduced value and usability.
• Customers should ensure that all data and opinions upon which they rely can be traced back through an unbroken chain of data based on ISO 17025.

Overview of ISO 17025 :

• ISO 17025 is one of the most popular quality standards for all laboratories; whether or not they do business with international customers. In 1891, British physicist Lord Kelvin wrote, “When you can measure what you are speaking about, and express it in numbers, you know something about it.? Mikel Harry, a noted Six Sigma authority, extends this thought as, “We don't know what we don’t know; we can’t act on what we don’t know; we won’t know until we search; we won’t search for what we don’t question; we don’t question what we don’t measure?. Both imply that if you failed to quantify the results of what you were doing, in a way, it means that you might not understand what you were really doing. Hence, organizations that are unable to track their processes, their products, or their raw materials are unable to fully manage their businesses.
• All other quality initiatives (eg. ISO 9001, QS-9001, TS-16949, Six Sigma, TQM, DOE, QFD, etc.) depend on reliable measurements, comparisons, and recommendations based on International Standards. ISO 17025 controls all aspects of how laboratories conduct their business (ie. who, what, when, where, how, how much, & why) of measurement, testing, certifying, recommending, & reporting.

ISO 17025 Success Factors :

• Research into what makes a ISO 17025 implementation a success has revealed 11 Critical Success Factors. They are, in order of importance :
• Top management leadership & commitment
• A simple, comprehensive implementation plan
• Training & support for everyone involved or affected by the implementation project
• Buy-in and voluntary support & commitment from a critical mass of people (>1 person, building to 25% of employees)
• Early successes that clearly prove that ISO 17025 will benefit customers, suppliers, management, and especially workers
• Adequate resources and time to achieve all that needs to be done
• Rapid and effective communication, feedback, and recognition on efforts made, results achieved, and work to be done
• Expert, pre-experienced advise, coaching, cheerleading, pre-warnings, and technical expertise on ISO 17025 implementation.
• Auditing, training, and remedial assistance to achieve consistent compliance to minimum requirements.
• Dress-rehersal audit, final fixes, then formal Registration Audit by Accredited Registrar
• Continuous assessment, improvement, and re-registration of systems.

How SSI Cert can help with you ISO 17025 Implementation? :

• Executive Overview Training for ISO 17025
• Project Planning, Scheduling, & Management
• Worker Training
• Generic Templates for Policies, Procedures, Process Maps, and Documentation Systems
• Statistical Data Analysis of 7 Characteristics of a Metrology System
• Repeatability5
• Reproducibility
• Linearity
• Bias
• Hysteresis
• Accuracy
• Granularity
• Calibration Models
• Inter-Lab Calibrations
• Reducing measurement system sensitivity to Operator, Environmental, Common cause, and Special Causes
• Developing Customized tests and measurement criteria.
• Error Reduction Investigations & Program Implementations
• Management Reviews for Accountability, Cost Reduction, and Independent (Third Party) Verification

HACCP is an abbreviation for Hazard Analysis Critical Control Point. It is implemented for identifying every potential risk in an industry. Assessing the maximum/minimum damage level of the risk, HACCP certifications determine the corrective measures in case the monitoring doesn’t show the critical limits. The procedures related to verification are included for managing the records effectively. At Ideal Quality Certifications, you can get prompt services and excellent results at pocket-friendly charges.

HACCP Principals :The implementation of hazard analysis Determine Critical Control Points (CCP). For each risk identified. Establishing critical limits, maximal and/or minimum value, by which biological, chemical and physical hazards in order to control the pedagogical prevention. Determination of procedures/processes for monitoring CCPs Determination of corrective measures in case the monitoring shows that the CCP is not within the critical limits. Establish procedures/processes for verification and certification procedures and the HACCP system is effective and it works well. The verification activities should be included authorized persons employed in production, the HACCP team. The establishment and effective management of records and documents.

If you are looking for GMP Certification Services in Mumbai (Maharashtra, India) then get in touch with Ideal Quality Certifications.  The purpose of this certification is to ensure that the pharmaceutical products are made according to the set quality standards. We are the name you can rely upon if you wish to get this certification. Backed by years of experience, we are familiar with all the legalities and quality standards that need to followed for it. We make sure that the client avoids making any mistake and attains this certification.

Benefits of GMP :

• It is believed that GMP is a good business tool, which will help to refine both compliance and performance of the Company. GMP requirements are largely common sense practices, which will help companies better itself as it moves toward a quality approach using continuous improvement.
• GMP is also sometimes referred to as “cGMP”. The “current, ” methodologies of manufacture, testing, design and control. The Manufacturers must employ technologies and systems, which are up-to-date. Systems and equipment used to prevent contamination, mixups, and errors are adequate by today’s standards. Thus, Good Manufacturing Practices GMP, when certified of an organization, is an authorization and certification of Companies product & process that quality standards are adequate, up to date and controlled for the intended use by the consumer.

How can DBS CERT help?

• DBS CERT consists of full-time trainers and certification with a unique combination of manufacturing experience, business and financial expertise,
• A “hands-on” approach creates a recipe for our clients’ success.
• System Study, Documentation-GMP Manual Preparation, Records Implementation, GMP Trainings, Internal Audits.

Clients choose us! :

• Bring world-class quality standards to your business :
  • Specialized in ISO certification, ISO Documentatiom, ISO Record, Iso Implementation, ISO Internal Auditing, ISO Certification, CE Marking, Training-Internal Auditing / is based in Mumbai, delhi, nce, India, Singapore, Tanzania, Nigeria, UK, Saudi Arabia, Sri Lanka, UAE.

ISO 13485:2016 Medical Certification Services is required to establish a Quality Management System (QMS), which is directed towards the development, design, production, and installation of medical devices and services related to it. ISO 13485 is important if you are dealing in medical devices and its related services. It ensures that the supplier can be trusted as he is registered and the products delivered are of top-quality. Get in touch with us now if you seek to attain this certification.

Use ISO 13485 :

• To establish a Quality Management System (QMS) that is oriented towards the design, development, production, and installation of medical devices and related services.
• To demonstrate your ability to supply medical devices and related services that meet customer expectations and comply with regulatory requirements.
• To evaluate how well your organization is able to meet customer expectations and comply with regulatory requirements.
• To become certified or registered.
• ISO 13485 is not a product standard. It’s a process standard. Therefore, it’s not enough to establish a Quality Management System (QMS) that complies with the ISO 13485 standard, you also need to comply with all relevant product and service oriented technical standards and regulations.

ISO 13485 Vs ISO 9001 :

• ISO 13485 is based on the ISO 9001 Quality Management standard. Both standards are organized in the same way and use basically the same numbering system. In addition, most of the ISO 13485 requirements are taken directly from ISO 9001 without modification.
• However, some ISO 9001 requirements were modified and others were excluded. Of course, ISO 13485 also includes a special set of requirements specifically related to the supply of medical devices and related services. In general, ISO 13485 is made up of two kinds of requirements: old ISO 9001 requirements and new requirements that are specifically related to medical devices and associated services.
• ISO 13485 excludes ISO 9001 requirements related to continual improvement and customer satisfaction. Continual improvement is excluded because most medical device regulations require organizations to maintain their Quality Management Systems, not to improve them. And customer satisfaction is excluded because committee members thought it was too subjective.

When ISO 9001 wants you to document a procedure, it also wants you to implement and maintain it. Section 4.2.1 of ISO 13485 expands on this idea by including requirements, activities, and special arrangements. More precisely :

• When ISO 13485 wants you to document a procedure, the standard also wants you to implement and maintain it.
• When ISO 13485 wants you to document a requirement, the standard also wants you to implement and maintain it.
• When ISO 13485 wants you to document an activity, the standard also wants you to implement and maintain it.
• When ISO 13485 wants you to document an arrangement, the standard also wants you to implement and maintain it.

ISO 29990:2010 sets out criteria for a quality management system standard for learning and training service providers including vocational institutions, corporations, and learning centers. ISO 2990:2010 Certification promotes the design of suitable services and evaluation of learning results. The aim of ISO 29990:2010 standard is to provide a generic model for excellent professional practice for learning service providers in the delivery of education and training programs.

Ideal Quality Certifications is a notable entity in the domain, successfully engaged in providing best-in-class ISO 29990:2010 certification services to the clients. Operating from Mumbai (Maharashtra), we are highly applauded among our clients for delivering reliable services. The offered services are rendered by our adroit professionals and they work according to the requirements of our clients to gain their maximum satisfaction. Besides, the ISO 29990:2010 certification services that we offer are available at market leading prices for our clients.

Quality Management System :Management system certification helps organization to continually improve through lessons learnt from past thereby to manage the present effectively & efficiently and planning to meet the challenges of future.

ISO 9001: 2015 :

• ISO 9001:2015 standard sets out the criteria for a quality management system that can be used by any organization, large or small, regardless of its field of activity.
• This standard is based on a number of quality management principles including a strong customer focus, the motivation and implication of top management, the process approach, risks & opportunities based thinking and to achieve continual improvement.
• Implementation of the standard is a means to demonstrate the organizations ability to consistently provide reliably quality products / services and build customer confidence.

ISO 9001:2015 brings a number of benefits :

• Focus on demonstration of leadership within the organization.
• Promotes Risk based thinking within the organization.
• Integration of QMS into business processes, as accountability of QMS, lies with top management.
• Due to focus on intended outcome i.e on desired output of process and associated risks and opportunities results in more reliable Product/Services for more effective and efficient service/product provision processes.
• Enhanced efficiency - With the ISO 9001 Certification, you can be assured of better performances within the company.
• Employees within organization would be working towards achiving the vision, mission, common goal of organization.
• Enhance the performance and productivity of each department and organization.
• High Morale among Employee.
• Builidng up of Excellent Brand Image.
• Certification Procedure :
• Application for certification from client (Submit Documents)
• Submission of offer by IQC
• Acceptance of Offer by client and Confirmation of agreement by both client organization and IQC
• Issuance of the “Certificate of approval” on successful completion of the initial / Re certification
• Validity of “Certificate of approval” is for three years from the date of decision, subject to conduct of annual Surveillance audits as agreed upon.
• before the expiry of “Certificate of approval”.
• Soft copy & hard copy within 3-4 days by dtdc courier.
• Your company details Check & verify online

ISO 29990:2010 sets out criteria for a quality management system standard for learning and training service providers including vocational institutions, corporations, and learning centers. ISO 2990:2010 Certification promotes the design of suitable services and evaluation of learning results. The aim of ISO 29990:2010 standard is to provide a generic model for excellent professional practice for learning service providers in the delivery of education and training programs.

Ideal Quality Certifications is a notable entity in the domain, successfully engaged in providing best-in-class ISO 29990:2010 certification services to the clients. Operating from Mumbai (Maharashtra), we are highly applauded among our clients for delivering reliable services. The offered services are rendered by our adroit professionals and they work according to the requirements of our clients to gain their maximum satisfaction. Besides, the ISO 29990:2010 certification services that we offer are available at market leading prices for our clients.