Quality

/Quality
Quality 2021-11-11T12:10:43+00:00
NADCAP 2021-07-28T07:28:48+00:00

Nadcap (formerly known as the National Aerospace and Defense Contractors Accreditation Program) is a worldwide cooperative program of major companies designed to manage a cost-effective consensus approach to special processes and products and provide continual improvement within the aerospace and defense industries.
Nadcap (National Aerospace and Defense Contractors Accreditation Program) is an industry-managed approach to conformity assessment of ‘special processes’ that brings together technical experts from prime contractors, suppliers and representatives from government to work together and establish requirements for approval
Nadcap is seen as the foremost standard for heat processing treatments in the aerospace industry. It helps to promote and maintain industrial standards and improves component quality. Furthermore, Nadcap gives customers more confidence and helps the industry to remain as safe as humanly possible.
The Nadcap accreditation process requires you to perform an internal audit – a form of self-assessment that is used to measure your strengths and weaknesses against the Nadcapaudit requirements [1] – and submit the results at least 30 days prior to the official audit.
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ISO 31000 – Risk management — Guidelines 2021-07-27T05:05:48+00:00

Organizations may face severe consequences in terms of economic performance and professional reputation, as well as environmental, safety and societal outcomes when they are unable to manage certain risks. Effective Risk Management helps organizations to perform well in an environment full of uncertainty.

ISO 31000 – Risk management Guidelines provides a framework for development, maintenance and improvement of an effective risk management in organizations as well as in global supply chains.

Elements of ISO 31000:

  • Communicate and consult.

  • Establish the context.

  • Identify risk.

  • Analyze risk.

  • Evaluate risk.

  • Treat risk.

  • Monitor and review

Principles of ISO 31000:

  • Creates value

  • Integral part of organizational processes

  • Part of decision making

  • Explicitly addresses uncertainty

  • Systematic, structured and timely

  • Based on the best available information

  • Tailored

  • Takes human and cultural factors into account

  • Transparent and inclusive

  • Dynamic, iterative and responsive to change

  • Facilitates continual improvement and enhancement of the organization

Benefits of ISO 31000:

  • 1. Objectives are achieved in given time.
    2. Risks are identified and treated throughout the organization.
    3. Identification of opportunities and threats.
    4. Compliance with relevant legal and regulatory requirements and international norms.
    5. Improved financial reporting.
    6. Improved governance.
    7. Improved stakeholder confidence and trust.
    8. Improved controls.
    9. Effectively allocates and uses resources for risk treatment.
    10. Improved operational effectiveness and efficiency.
    11. Enhanced health and safety performance, as well as environmental protection.
    12. Improved loss prevention and incident management.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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IRIS – International Railway Industry Standard 2021-07-27T05:06:10+00:00

The International Railway Industry Standard (IRIS) is an internationally recognized management system standard specific to the railway industry. It is based on the ISO 9001 structure, but stipulates additional, railway- specific requirements for business management systems.

What are the Benefits of IRIS Certification?
Simplified supplier evaluation and approval processes

  • Save time and money by eliminating individual supplier qualifications

  • Offer web-based availability of your certification information to your current and prospective customers

  • Improved product quality

  • Potential to combine certification with ISO 9001

  • Six Steps to Attain IRIS Certification:
    1. Preparation for IRIS certification
    2. Readiness review (suggested)
    3. Initial certification audit
    4. Three-year IRIS certificate issuance
    5. Periodic surveillance audits
    6. Upon expiration, recertification audit

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 13485 – Medical devices — Quality management systems — Requirements for regulatory purposes 2021-07-27T05:06:35+00:00

ISO 13485:2016 Medical devices – Quality Management System Requirements for regulatory purposes represents the requirements that medical device manufacturers must incorporate into their management systems. Though based on ISO 9001, ISO 13485 removes 9001’s emphasis on continual improvement and customer satisfaction. In its place, emphasis is on meeting regulatory as well as customer requirements, risk management and maintaining effective processes. ISO 13485 standard is in part designed to produce a management system that facilitates compliance to the requirements of customers and, pre-eminently, various global regulators.

While being certified to ISO 13485 does not fulfill the requirements of either the FDA or other foreign regulators, the certification aligns an organization’s management system to the requirements of the FDA’s Quality System Regulation (QSR) requirements as well as many other regulatory requirements found throughout the world. Therefore, ISO 13485:2016 certification serves to create a management system that can be thought of as a framework on which compliance to various regulatory and customer requirements have to be build.

ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose.

The benefits of management systems certification:
Your management system’s conformity with ISO 13485 can help your company open doors to untapped domestic and international business opportunities, and reap the benefits of:

  • Expanded market access – National regulatory authorities require or strongly prefer that manufacturers marketing medical products in their countries have a third-party audited and certified management system in place. Investing in such a system speeds access into those countries that require it, and expedites market entry into the others.
  • Reduced cost of sales – Your certification establishes your company’s credibility and commitment to quality. Because the task of explaining the specifics and demonstrating the effectiveness of your quality system is more straightforward, it takes less time to earn your prospective customers’ trust and confidence.
  • Improved performance – Based on a uniform and widely-accepted system of process control, your company’s certified management system helps you improve your products and processes. This can foster improved relationships with your suppliers, business partners, and customers, and give you a real advantage in the marketplace.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 10015 – Quality management — Guidelines for competence management and people development 2021-07-27T05:06:49+00:00

Managing human resources is a critical and no less than a herculean task in the organization. Experts say that lack of appropriate management system results in inefficient handling of human capital. ISO 10015 standards help in achieving it in a better and enhanced way. The training program not only gives the basics of it but also gives an in-depth understanding of the role of HR in the company. We are a sought-after training institute backed by a pool of proficient ISO 10015 practitioners with in depth expertise and years of experience.

Why should attend the training Program:
ISO 10015 certification program is useful for everyone who is involved in the analysis and design of human capital management. People who design the training management system in the company or those who audit the human resource management are vastly benefited by it.

ISO 10015 offers guidance to organizations for identifying and analyzing the training needs. It also tells the ways of designing and planning the same. Organizations learn how to evaluate the outcomes of a training program and how to monitor the effectiveness of it? We teach everything about ISO 10015 so that HR Managers and senior leaders of an organization make the best use of our training solutions.

Benefits of Training Program:
You can count on our comprehensive training program for the best learning about the relevance and use of training in the organization. If your organization has already implemented ISO 9001, then you get a tremendous improvement in the HR system after attending the training program. We also offer bespoke training solutions to match with the objectives of your organization.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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NABH – National Accreditation Board for Hospitals & Healthcare Providers (NABH) 2021-07-27T05:07:05+00:00

NABH is an acronym for National Accreditation Board for Hospitals & Healthcare Providers. It is a constituent board of Quality Council of India, set up to establish and operate accreditation program for healthcare organizations.
Accreditation is a process of reviewing in which healthcare organizations participate to demonstrate the ability to meet predetermined criteria and standards of accreditation established by a professional accrediting agency.

Why you need NABH Accreditation?

  • Commitment to create a culture of quality, patient safety, efficiency and accountability towards patient care.

  • Establishment of protocols and policies as per National/International Standards for patient care, medication management, consent process, patient safety, clinical outcomes, medical records, infection control and staffing.

  • Patients are treated with respect, dignity and courtesy at all times. Patients are involved in care planning and decision making.

  • Patients are treated by qualified and trained staff. Feedback from patients is sought and complaints (if any) are addressed.

  • Transparency in billing and availability of tariff list. Continuous monitoring of its services for improvement.

  • Commitment to prevent adverse events that may occur.

Contents of NABH Standard:

  • Access, Assessment and continuity of care (AAC)

  • Patient Right and Education (PRE).

  • Care of Patients (COP).

  • Management of Medication (MOM).

  • Hospital Infection Control (HIC).

  • Continuous Quality Improvement (CQI)

  • Responsibility of Management (ROM).

  • Facility Management and Safety (FMS).

  • Human Resource Management (HRM)

  • Information Management System (IMS).

Benefits of NABH Accreditation:

  • Accreditation benefits all Stake Holders. Patients are the biggest beneficiaries. Accreditation results in high quality of care and patient’s safety. The patients get services by credential medical staff. Rights of patients are respected and protected. Patient satisfaction is regularly evaluated.

  • Accreditation to a Hospital stimulates continuous improvement. It enables hospital in demonstrating commitment to quality care. It raises community confidence in the services provided by the hospital. It also provides opportunity to healthcare unit to benchmark with the best.

  • The Staff in an accredited hospital are satisfied lot as it provides for continuous learning, good working environment, leadership and above all, ownership of clinical processes. It improves overall professional development of Clinicians and Paramedical staff and provides leadership for quality improvement within medicine and nursing.

  • Accreditation provides an objective system of empanelment by insurance and other Third Parties. Accreditation provides access to reliable and certified information on facilities, infrastructure and level of care.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 37500 – Guidance on outsourcing 2021-07-27T05:07:21+00:00

ISO 37500 covers the main phases, processes and governance aspects of outsourcing, independent of size and sectors of industry and commerce. It is intended to provide a good foundation to enable organizations to enter into, and continue to sustain, successful outsourcing arrangements throughout the contractual period.

Why ISO 37500?

  • outsourcing governance for mutual benefit for client and provider;

  • flexibility of outsourcing arrangements, accommodating changing business requirements;

  • identifying risks involved with outsourcing;

  • enable mutually beneficial collaborative relationships.

ISO 37500 Contents:

  • Scope

  • Normative references

  • Terms and definitions

  • Outsourcing introduction and model

  • Outsourcing governance and framework

  • Phase 1: outsourcing strategy analysis

  • Phase 2: initiation and selection

  • Phase 3: transition

  • Phase 4: delivery value

Benefits of ISO 37500:

  • decision makers and their empowered representatives;

  • all stakeholders engaged in facilitating the creation and/or management of outsourcing arrangements;

  • staff at all levels of experience in outsourcing;

  • those individuals or organizations who are outsourced, thus enabling the client and provider to operate under a common level of understanding

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 15489-1- Information and documentation — Records management — Part 1: Concepts and principles 2021-07-27T05:07:35+00:00

The International Standard on Records Management, ISO 15489, was launched in October 2001 at the Association of Records Management and Administrator’s (ARMA) International Conference in Montreal and get revised to latest version in 2016. This part of ISO 15489 applies to the creation, capture and management of records regardless of structure or form, in all types of industries/sectors and technological environments, over time.

  • applies to the management of records, in all formats or media, created or received by any public or private organization in the conduct of its activities, or any individual with a duty to create and maintain records

  • provides guidance on determining the responsibilities of organizations for records and records policies, procedures, systems and processes,

  • provides guidance on records management in support of a quality process framework to comply with ISO 9001 and ISO 14001,

  • provides guidance on the design and implementation of a records system, but

  • does not include the management of archival records within archival institutions

AIM:

To ensure that adequate records are created, captured and managed.

Principles of Record Management:

  • Records are created to support business activity, provide accountability, and comply with regulatory environments.

  • Records management rules should be embedded in all business processes requiring documentation.

  • Business continuity should ensure identification and protection of vital records.

Requirement of ISO 15489:

  • Relevant organizational structure chart

  • Mission statements for organization and/or department

  • Records management mission statement

  • Records management policy

  • Records management procedures (might be a manual) used by the records management team, including any in-house training material or details of other training

  • Specifications for automated records management systems for paper records

  • Specifications of records management systems for digital records

  • Retention schedules

  • Access authorizations

  • Accession records

  • Documentation on records destruction or contracted-out services

  • Written specifications for shelving, boxing, and storage facilities

  • Vital records inventory

  • Vital records protection procedures, including recovery in event of disaster

  • Business continuity plan

  • Agreements with any third-party service providers for business continuity services

  • Surrogacy program documentation

  • Staff job descriptions both within and outside records management team

Benefits of ISO 15489:

  • conduct business in an orderly, efficient and accountable manner,

  • deliver services in a consistent and equitable manner,

  • support and document policy formation and managerial decision making,

  • provide consistency, continuity and productivity in management and administration,

  • facilitate the effective performance of activities throughout an organization,

  • provide continuity in the event of a disaster,

  • meet legislative and regulatory requirements including archival, audit and oversight activities,

  • provide protection and support in litigation including the management of risks associated with the existence of, or lack of, evidence of organizational activity,

  • protect the interests of the organization and the rights of employees, clients and present and future stakeholders,

  • support and document current and future research and development activities, developments and achievements, as well as historical research,

  • provide evidence of business, personal and cultural activity,

  • establish business, personal and cultural identity, and

  • maintain corporate, personal or collective memory.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 29001- Petroleum, petrochemical and natural gas industries — Sector-specific quality management systems — Requirements for product and service supply organizations 2021-07-27T05:07:51+00:00

ISO/TS 29001 is a company level certification based on a technical specification published by the International Organization for Standardization (ISO) titled “Petroleum, petrochemical and natural gas industries — Sector-specific quality management systems — Requirements for product and service supply organizations”. The document was developed with cooperation from the American Petroleum Institute (API). The technical specifications include ISO 9001 in its entirety and specific requirements for the petroleum, petrochemical and natural gas industries. The current version of this standard is ISO/TS 29001:2010.

This certification is for organizations involved in exploration, production, pipelines and transport, refining of petroleum and natural gas and those that provide technical and support services to these industries. The specification is also applicable to manufacturers and purchasers of oil, and gas industry equipment can also use this technical specification.

Requirements of ISO 29001:

  • Design and development

  • production

  • installation services

  • internal audit

  • management review meeting

  • field non conformity analysis

  • fulfill the management requirements of ISO 9001

Benefits of ISO 29001:

  • Customer loyalty

  • Repeat business and referral

  • Operational results such as revenue and market share

  • Flexible and fast responses to market opportunities

  • Costs and cycle times through effective and efficient use of resources

  • Alignment of processes which will best achieve desired results

  • Competitive advantage through improved organizational capabilities

  • Understanding and motivating people towards the organization’s goals and objectives, as well as participation in continual improvement

  • Confidence of interested parties in the objectiveness and efficiency of the organization, as demonstrated by the financial and social benefits from the organization’s performance, product life cycle, and reputation

  • Ability to create value for both the organization and its suppliers by optimization of costs and resources as well as flexibility and speed of joint responses to changing markets.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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ISO/IEC 17020 Conformity assessment — Requirements for the operation of various types of bodies performing inspection 2021-07-27T05:08:11+00:00

Inspection body accreditation is the procedure by which an authoritative body gives a formal recognition that an inspection body is competent and impartial to carry out the inspection service according to ISO/IEC 17020. The objective of accreditation is to assure the clients of the quality of the inspection service of the inspection body as well as to avoid duplicate inspection. Examples of the inspection bodies are those for boilers in factories, liquid petroleum gas, pressure vessels, Used cars, pre-shipment inspection body, etc.

To apply for accreditation, the inspection body must comply with the standard ISO/IEC 17020 General Criteria for the Operation of Various Types of Bodies Performing Inspection.

Inspection Body :- is a body which carries out the examination of the product design, product, service, process or plant, and determination of their conformity with specific requirements or general requirements. The inspection body shall be legally identifiable, and shall have documentation which describes its functions and the technical scope of activity for which it is competent.

Type of Inspection Body :- Inspection body can be classified into 3 types as follows :
Type A inspection body is the inspection body which provides “third party” inspection service. The inspection body and its staff shall not engage in any activities that may conflict with their independence of judgement and integrity in relation to their inspection activities.
Type B inspection body is the inspection body which forms a separate and an identifiable part of an Organization and has been established to supply inspection services to its parent organization.
Type C inspection body is the inspection body which forms an identifiable part of an organization and has been established to supply inspection services to its parent organization and other external organizations.
Therefore, inspection body can be an organization or part of an organization.

Overview of ISO 17020
The requirements of ISO 17020 are contained in 14 major sections including:

  • Administrative requirements

  • Requirements for independence, impartiality, and integrity

  • Confidentiality

  • Organization and management

  • Quality system

  • Personnel

  • Facilities and equipment

  • Inspection methods and procedures

  • Handling of inspection samples and items

  • Control of records

  • Inspection reports and inspection certificates

  • Subcontracting

  • Complaints and appeals

  • Cooperation with other inspection bodies

Like ISO 9001 and ISO 17025, ISO 17020 requires procedures in several important areas, including:
Procedure to ensure that persons or organizations external to the inspection body cannot influence the results of inspections by the ISO 17020-accredited organization

  • Procedure for feedback

  • Procedure for corrective action

  • Procedure for the care and maintenance of equipment

  • Procedure for selecting qualified suppliers

  • Procedure for purchasing

  • Procedure for inspection of materials received by the organization

  • Procedure for appropriate storage facilities

  • Procedure for protecting the integrity of data produced by the organization

  • Procedure for ensuring the security of data produced by the organization

  • Procedure for dealing with defective equipment

  • Procedure(s) for performing inspections

  • Procedure(s) for performing non-standard inspections

  • Procedure(s) for avoiding deterioration or damage to inspection items

  • Procedure for dealing with complaints

  • Procedure for dealing with appeals against the results of inspections

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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ISO 15189 – Medical laboratories — Requirements for quality and competence 2021-07-27T05:08:30+00:00

ISO 15189 specifies requirements for quality and competence in medical laboratories. ISO 15189 can be used by medical laboratories in developing their quality management systems and assessing their own competence.
The requirements for ISO 15189 medical laboratory accreditation are divided into two parts, technical requirements and management requirements.

The Medical Laboratories Management Requirements for ISO Certified are:

  • Organization and Management

  • Document Control

  • Examination by Referral Laboratories

  • Advisory Services

  • Identification and Control of Nonconformities

  • Preventive Action

  • Quality and Technical Records

  • Management Review

  • Quality Management System

  • Review of Contracts

  • External Services and Supplies

  • Resolution of Complaints

  • Corrective Action

  • Continual Improvement

  • Internal Audits

The Technical Requirements in Medical Laboratories for ISO certified are:

  • Personnel

  • Lab equipment

  • Examination procedures

  • Post-examination procedures

  • Accommodation and environmental conditions

  • Pre-examination procedures

  • Assuring quality of examination procedures

  • Reporting of results

Benefits

ISO 15189 implementation improves / leads to

  • POLICIES & OBJECTIVES set by ‘top management’

  • Conformance to Legal and Regulatory Requirements

  • Recognition by regulators around the world of ISO 15189 as a good basis for addressing medical device design and manufacturing regulatory requirements

  • Controlled consistency of manufactured products

  • Managed productivity and efficiency, controlling costs

  • Competitive advantage and increased marketing and sales opportunities.

  • Improved customer perception of the organization’s image, culture and performance.

  • improved internal and external Communications

  • greater understanding of the organization’s processes

  • clear responsibilities and authorities agreed for all staff

  • improved use of time and resources

  • reduced wastage

  • greater consistency and traceability of products and services

  • Customer Confidence, Satisfaction and TRUST

  • Level of Assurance in Organizational QUALITY

  • Organizational PROFITABILITY

  • Ability to Differentiate Organization for Competitive Advantage

  • Organizational Credibility & Reputation

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
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ISO 29990 – Learning services for non-formal education and training — Basic requirements for service providers 2021-07-27T05:10:38+00:00

ISO 29990 aims to establish an overall quality model for professional practice and performance, as well as a common reference for teaching their customers the planning, development and implementation of education and training, as well as the promotion of development. The standard focuses on the learner, learning outcomes, learning service.
The standard is aimed at organizations that have an education.

Requirements for ISO 29990:

  • All clause requirements of the International Standards ISO 9001
  • Determining the learning needs

  • Design of learning services

  • Provision of learning services

  • Monitoring of learning services

  • Evaluation by teaching

Benefits of ISO 29990:

  • Transparency/comparability of offers

  • Liability of the offers

  • Information about criteria for assessment of studying offers

  • Optimized processes

  • Improved learning environment

  • Provision of resources, including trainer with sufficient competencies

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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AS 9120 – Quality Management Systems – Aerospace Requirements for Stockist and Distributors 2021-07-27T05:11:30+00:00

AS 9120 is a company level certification based on a standard published by the Society of Automotive Engineers (SAE) titled “Quality Management Systems-Aerospace Requirements for Stockist / Distributors”. This standard includes ISO 9001 and specific requirements related to the Aerospace Industry.

AS 9120 requirements are based on 9001 standards. As it applicable only to distributor, some of the requirements are

  • Awareness of contribution to compliance and product safety.
  • Control of product obsolescence
  • Prevention of counterfeit parts
  • Product identification and traceability
  • Consider human factors in Non conformance

Benefits

  • Customer satisfaction improved
  • Well defined and documented procedures improve the consistency of output

  • Quality is constantly measured

  • Procedures ensure corrective action is taken whenever defects occur
  • Non conformity rates decrease

  • Non conformity are caught earlier and are corrected at a lower cost

  • Defining procedures identifies current practices that are obsolete or inefficient

  • Documented procedures are easier for new employees to follow

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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ISO/IEC 17025 – General requirements for the competence of Testing and Calibration Laboratories 2021-07-27T05:11:43+00:00

ISO/IEC 17025 is a company level accreditation based on a standard published by the International Organization for Standardization (ISO) titled “General requirements for the competence of testing and calibration laboratories”. This accreditation is specific to a scope.

ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent.

It confirms that a particular laboratory is able to produce precise and accurate test results and calibration data, including: Traceability of measurements and calibrations to national standards.

Steps to ISO/IEC 17025 Accreditation

  • Learn about the Standard.
  • Perform a Gap Analysis.
  • Plan your project.
  • Train your organization.
  • Document your Quality Management System.
  • Implement your QMS and conduct business.
  • Audit your QMS.
  • Accreditation Audit.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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AS 9110 – Quality Maintenance Systems – Aerospace – Requirements for Maintenance Organizations 2021-07-27T05:12:07+00:00

AS9110 is a standard that defines the quality system requirements for organizations whose primary business is in the aircraft industry at all levels of the maintenance, repair & overhaul (MRO) process. It is focused on the control of repair schemes and maintenance plans, configuration management, and the skills and qualifications necessary to perform MRO tasks within the aerospace community.

Based on ISO 9001 but with nearly 100 additional requirements specific to the aerospace MRO industry, AS9110 provides suppliers with a comprehensive quality system focused on areas directly impacting product safety and reliability, such as:

  • Discusses civil aviation authorities and where in the standard that those requirements apply
  • Defines terms unique to the MRO industry such as maintenance, technical data, human factors, and release certificates
  • Expanded requirements for personnel conducting MRO task
  • Addresses the qualification of new maintenance processes

MRO must meet the requirements of the Federal Aviation Regulation (FAR) Part 43 & 145, the Civil Aviation Administration of China and the European Authority for aviation safety. This includes approvals, ratings, licenses and permits. MRO also needs to have approvals for certain types of repairs, rated on the specific airframe and/or engine platform, and carry the appropriate regulatory certificates.

Benefits of AS9110 Certification for your organization:

  • Reduced costs due to improved product reliability
  • Better process control and flow
  • Better documentation of processes
  • Greater employee quality awareness
  • Reductions in product scrap, rewords, and rejections

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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AS 9100 D – Quality Management System for Aviation, Space and Defense Organizations 2021-07-27T05:12:21+00:00

AS9100 is an international standard containing requirements for establishing and maintaining a quality management system for the aerospace industry. AS9100 is used by organizations that design, develop, and produce aviation, space, and defense products.

While primarily developed for the aviation, space and defense industry, this standard can also be used in other industry sectors when a quality management system with additional requirements over an ISO 9001:2015 system is needed.

Steps to AS9100 Certification

  • Learn about the Standard.
  • Perform a Gap Analysis.
  • Plan your project.
  • Train your organization.
  • Document your Quality Management System.
  • Implement your QMS and conduct business.
  • Audit your QMS.
  • Registration Audit.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

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IATF 16949: Quality Management System for Automotive Industry 2021-07-27T05:12:46+00:00

What is IATF 16949?

IATF 16949:2016 is the International Standard for Automotive Quality Management Systems. IATF 16949 was jointly developed by The International Automotive Task Force (IATF) members and submitted to the International Organization for Standardization (ISO) for approval and publication. The document is a common automotive quality system requirement based on ISO 9001, and customer specific requirements from the automotive sector.
IATF 16949 emphasizes the development of a process-oriented quality management system that provides for continual improvement, defect prevention and reduction of variation and waste in the supply chain. The goal is to meet customer requirements efficiently and effectively.
Who is it applicable to?

The standard is applicable to any organization that manufactures components, assemblies and parts for supply to the automotive industry. In this context manufacturing is defined as:
The process of making or fabricating production materials, production or service parts, assemblies or heat treatment, welding, painting, plating or other finishing services.

Benefits of IATF 16949

  • Credibility and image. …
  • Credibility to supply the automotive industry. …

  • Improvement. …
  • Process approach. …
  • Decision making. …
  • Continual improvement. …
  • Employee motivation and empowerment.

Training/Certification/Assessment/ Consultancy Services:

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

Contact us
Training/Certification/Assessment/ Consultancy Services: 2021-07-27T05:12:59+00:00

System Certifications Inc. is one of the largest and leading consultants in India. We provide quick, result oriented and easy to implement consultation and training services for applicable standards.

We have been associated with organizations across the India for their ISO standard certification projects.
For more Details and Consultation/ Training Services please contact us:

Contact us
ISO 9001- Quality Management System 2021-04-23T07:37:18+00:00

ISO 9001 is defined as the international standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements.

ISO 9001 is the world’s most recognized Quality Management System (QMS) standard. Its aim is to help organizations meet the needs of their customers and other stakeholders more effectively. This is achieved by building a framework to ensure consistent quality in the provision of goods and/or services.

  • Suitable for both small and large organizations
  • Better internal management.
  • Less wastage.
  • Increase in efficiency, productivity and profit.
  • Improved customer retention and acquisition.
  • Consistent outcomes, measured and monitored.
  • Globally recognized standard.
  • The seven quality management principles are:
  • Customer focus.
  • Leadership.
  • Engagement of people.
  • Process approach.
  • Improvement.
  • Evidence-based decision making.
  • Relationship management.

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