BEST ISO 9001 CERTIFICATION IN NANGLOI, DELHI

BEST ISO 9001 CERTIFICATION IN NANGLOI, DELHI

Ultimate Quality Solutions Provide consultancy services for ISO 9001 Quality Certifications for your esteemed organization. We very much appreciate for your positive thinking and long term vision for growth in today’s competitive environment. Global market access depends on compliance with international standards in performance, product and service.

Why Ultimate Quality Solutions Best ISO 9001 Certification in Nangloi, DELHI

Ultimate Quality Solutions is a training and consultancy organization formed with the objective of promoting sustainable industrial Development. We have Assisted many organizations to Enhance their Business Performance in a Global competitive liberalized economy in India. Due to this emerging need we focus our services for improvement in Quality performance, Customer satisfaction and Cost control through the ISO 9001, 14001, 22000, 27000, OHSAS 18001 etc.                                                                           

Ultimate Quality Solutions provides wide range of services with an experienced and well trained Lead Auditors and have got their clients certified from world’s leading organizations such as - DAC (UAE), JAS-ANZ (Australia), UKAS (UK), NABCB, etc.

Ultimate Quality Solutions provides fully integrated IT Enabled Quality Solutions conceptualized and developed by professionals in the area of quality management with extensive experience in implementing and auditing quality systems worldwide. Advantages of the solution proposed by us are:

1. Ultimate Quality Solutions has Process Modal and Structured approach to establish performance indicators so that continual improvement can take place and sustain itself in terms of productivity, profitability and customer satisfaction.
2. Ultimate Quality Solutions is both training and consultancy organization.
3. Ultimate Quality Solutions are Engineering, Environmental & Management Professionals with vast experience in various industries of diverse fields such as Automobile, Bank, IT, Education, Engineering, Electrical, Electronic, Textile, Petro, Power, Food and Service industries.
4. Ultimate Quality Solutions are involved for Development, Implementation and Auditing of Quality systems for ISO 9001, 14001, 22000, 27000, HACCP, OHSAS 18001 etc.
5. Ultimate Quality Solutions systems prevent organization paying “High Cost for Low Quality Data”, which is in consistent irreconcilable, thus saving countless unproductive hours to reconcile them.
6. Ultimate Quality Solutions provides value added services for ISO 9001:2015 certifications only to recognition looking for improvement and is not an agent for ISO Certification
7. Ultimate Quality Solutions offer WIN-WIN-WIN situation for Organization, Consultant and Customer by

• Faster Certification
• Continual Improvement Process
• Reduced Documentation
• Better Data Analysis
• Increased productivity
• Enhanced staff motivation
• Competitive advantage
• More effective use of resources
• Enhanced customer satisfaction&

We believe in uploading highest standards of business ethics with complete commitment to total quality. We take great pride in the confidence and respect that we have earned from our clients and strive to improve every day.

   

Time Frame for ISO 9001 Certification

The work related to preparation & implementation of QUALITY Management Systems can be completed in a period of approximately 10 to 15 DAYS. However for this purpose, it is essential that your management responds favorably to our consultant’s advice and is able to take recommended actions within the prescribed time-frame.

                                                                                                      

BEST ISO 9001 Certification in Nangloi Just in Rs 3999/-, DELHI

The fee shall be payable by you in installments as per the completion of work in different modules.

Advance with application                                50%

After getting soft copy of the certificate          50%

We shall be charging a fee of /- as Surveillance audit fees annul.

You will organize your own computer, photocopier, stationary and other related facilities for the preparation of documents.

Any other expenditure to be incurred on development of QMS, like procurement of any machinery, test equipment, calibrations, materials, etc. shall be borne by .

Mode of Payment for ISO 9001 CERTIFICATION 

Cheque, NEFT or Demand Draft in favor of “Ultimate Quality Solutions”, Payable at New Delhi only.

Documents Required For ISO 9001 CERTIFICATIONS               

 ·        Application Form:

 ·        Company Profile:

 ·        PAN Card (Company or Proprietor):

 ·        Company or Firm Registration certificate (if any)

 ·        Services Tax or VAT or Sales Tax : (if any)

 ·        Product list with product Description.

 ·        List of Company Employees (any 5 to 8 Employees):

 ·        Name – Designation – Qualification – Experience.

 ·        Hand written Name, Address and Scope on Letter head or Plain paper with confirmation sign.

What is an ISO 13485 Quality Management System?

ISO 13485:2013 Medical Devices (QUALITY MANAGEMENT SYSTMS)

FOR

What is an ISO 13485 Quality Management System?

ISO 13485 is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 quality management standard series. ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. While ISO 13485 is based on the ISO 9001 process model concepts of Plan, Do, Check, Act, it is designed for regulatory compliance. It is more prescriptive in nature and requires a more thoroughly documented quality management system.
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.

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What are the benefits of being certified to ISO 13485?

Whether you are looking to operate internationally or expand locally, ISO 13485 Certification can help you improve overall performance, eliminate uncertainty, and widen market opportunities. Companies with this certification communicate a commitment to quality to both customers and regulators.

• Increase access to more markets worldwide with certification
• Outline how to review and improve processes across your organization
• Increase efficiency, cut costs and monitor supply chain performance
• Demonstrate that you produce safer and more effective medical devices
• Meet regulatory requirements and customer expectations

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ISO 13485, CMDR, FDA and CE marking services from a Notified Body

ISO 13485 is the best internationally-accepted model a medical device organization can implement to help demonstrate compliance to laws and regulations of the medical device industry. ISO 13485 is the quality management system standard accepted as the basis for CE marking medical devices under European Directives. Increasingly, ISO 13485 is being required, or is at least beneficial, in supporting regulations around the world, including the Health Canada Canadian Medical Device Regulations CMDCA What is an ISO 13485 Quality Management System?

ISO 13485 is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 quality management standard series. ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. While ISO 13485 is based on the ISO 9001 process model concepts of Plan, Do, Check, Act, it is designed for regulatory compliance. It is more prescriptive in nature and requires a more thoroughly documented quality management system.
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.

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What are the benefits of being certified to ISO 13485?

Whether you are looking to operate internationally or expand locally, ISO 13485 Certification can help you improve overall performance, eliminate uncertainty, and widen market opportunities. Companies with this certification communicate a commitment to quality to both customers and regulators.

• Increase access to more markets worldwide with certification
• Outline how to review and improve processes across your organization
• Increase efficiency, cut costs and monitor supply chain performance
• Demonstrate that you produce safer and more effective medical devices
• Meet regulatory requirements and customer expectations

---

ISO 13485, CMDR, FDA and CE marking services from a Notified Body

ISO 13485 is the best internationally-accepted model a medical device organization can implement to help demonstrate compliance to laws and regulations of the medical device industry. ISO 13485 is the quality management system standard accepted as the basis for CE marking  medical devices under European Directives Increasingly, ISO 13485 is being required, or is at least beneficial, in supporting regulations around the world, including the Health Canada Canadian Medical Device Regulations CMDCAS programme.
Although ISO 13485 certification is not a direct requirement for CE marking medical devices under the European Medical Device Directives, it is recognized as a harmonized standard by the European Commission. As one of the leading notified bodies for CE marking, we can support you on selecting the most efficient conformity assessment routes to achieve CE marking.
BSI ISO 13485 Certification is one component of the comprehensive portfolio of quality management assurance services that we provide, together with our toll
Popular services that compliment ISO 13485 include:
Programme.
Although ISO 13485 certification is not a direct requirement for CE marking medical devices under the European Medical Device Directives, it is recognized as a harmonized standard by the European Commission. As one of the leading notified bodies for CE marking, we can support you on selecting the most efficient conformity assessment routes to achieve CE marking.
BSI ISO 13485 Certification is one component of the comprehensive portfolio of quality management assurance services that we provide, together with our BSI Excellerator tool.
Popular services that compliment ISO 13485 include:

Time Frame

The work related to preparation & implementation of QUALITY Management Systems can be completed in a period of approximately 10 to 15 DAYS. However for this purpose, it is essential that your management responds favorably to our consultant’s advice and is able to take recommended actions within the prescribed time-frame.

Terms & Conditions

1.    We shall be charging our total fee (consultancy fee and certification fee).as per as follows

   S. no.                 Fees                Certification               Board             Scope

          01.                     25,000             13485:2013                 UK                   (Q.M.S) 

   

                                                                                                     

Note:-

We will charge extra /- per man days for implement of Your Company.

1.    The fee shall be payable by you in installments as per the completion of work in different modules.

1.    Advance with application                                50%

2.    After getting softcopy of the certificate          50%

1.    We shall be charging a fee of /- as Surveillance audit fees per annum.

1.    You will organize your own computer, photocopier, stationary and other related facilities for the preparation of documents.

1.    Any other expenditure to be incurred on development of QMS, like procurement of any machinery, test equipment, calibrations, materials, etc. shall be borne by .

ISO 27001:2013 (INFORMATION SECURITY MANAGEMENT SYSTMS)

ISO 27001:2013 (INFORMATION SECURITY MANAGEMENT SYSTMS)

FOR

What is ISO/IEC 27000 family - Information security management systems

The ISO/IEC 27000 family of standards helps organizations keep information assets secure.

Using this family of standards will help your organization manage the security of assets such as financial information, intellectual property, employee details or information entrusted to you by third parties.

ISO/IEC 27001 is the best-known standard in the family providing requirements for an information security management system (ISMS).

There are more than a dozen standards in the 27000 family.

What is an ISMS?

An ISMS is a systematic approach to managing sensitive company information so that it remains secure. It includes people, processes and IT systems by applying a risk management process.

It can help small, medium and large businesses in any sector keep information assets secure.

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What is ISO 27001?

ISO 27001 (formally known as ISO/IEC 27001:2005) is a specification for an information security management system (ISMS). An ISMS is a framework of policies and procedures that includes all legal, physical and technical controls involved in an organization’s information risk management processes.

According to its documentation, ISO 27001 was developed to "provide a model for establishing, implementing, operating, monitoring, reviewing, maintaining and improving an information security management system."

ISO 27001 uses a top down, risk-based approach and is technology-neutral. The specification defines a six-part planning process:

1. Define a security policy.
2. Define the scope of the ISMS.
3. Conduct a risk assessment.
4. Manage identified risks.
5. Select control objectives and controls to be implemented.
6. Prepare a statement of applicability.

The specification includes details for documentation, management responsibility, internal audits, continual improvement, and corrective and preventive action. The standard requires cooperation among all sections of an organization.

The 27001 standard does not mandate specific information security controls, but it provides a checklist of controls that should be considered in the accompanying code of practice, ISO/IEC 27002:2005. This second standard describes a comprehensive set of information security control objectives and a set of generally accepted good practice security controls.

ISO 27002 contains 12 main sections:

1. Risk assessment
2. Security policy
3. Organization of information security
4. Asset management
5. Human resources security
6. Physical and environmental security
7. Communications and operations management
8. Access control
9. Information systems acquisition, development and maintenance
10. Information security incident management
11. Business continuity management
12. Compliance

Organizations are required to apply these controls appropriately in line with their specific risks. Third-party accredited certification is recommended for ISO 27001 conformances.

Other standards being developed in the 27000 family are:

• 27003 – Implementation guidance.
• 27004 - an information security management measurement standard suggesting metrics to help improve the effectiveness of an ISMS.
• 27005 – an information security risk management standard. (Published in 2008)
• 27006 - a guide to the certification or registration process for accredited ISMS certification or registration bodies. (Published in 2007)
• 27007 – ISMS auditing guideline.

Terms & Conditions

1.    We shall be charging our total fee (consultancy fee and certification fee).as per as follows

   S. no.                 Fees                Certification               Board             Scope

          01.                     25,000             27001:2013                 DEC                (Q.M.S) 

    01.                     15,000             27001:2013                 UK Cert          (Q.M.S)

                                                                                                     

Note:-

We will charge extra 3,000/- per man days for implement of Your Company.

1.    The fee shall be payable by you in installments as per the completion of work in different modules.

1.    Advance with application                                50%

2.    After getting soft copy of the certificate          50%

1.    We shall be charging a fee of /- as Surveillance audit fees per annum.

1.    You will organize your own computer, photocopier, stationary and other related facilities for the preparation of documents.

1.    Any other expenditure to be incurred on development of QMS, like procurement of any machinery, test equipment, calibrations, materials, etc. shall be borne by .

Mode of Payment

Cheque or Demand Draft in favor of “Ultimate Quality Solutions”, Payable at New Delhi only.

WHY Ultimate Quality Solutions?

Ultimate Quality Solutions provides fully integrated IT Enabled Quality Solutions conceptualized and developed by professionals in the area of quality management with extensive experience in implementing and auditing quality systems worldwide. Advantages of the solution proposed by us are:

1.    Ultimate Quality Solutions has Process Modal and Structured approach to establish performance indicators so that continual improvement can take place and sustain itself in terms of productivity, profitability and customer satisfaction.

1.    Ultimate Quality Solutions is both training and consultancy organization.

1.    Ultimate Quality Solutions are Engineering, Environmental & Management Professionals with vast experience in various industries of diverse fields such as Automobile, Bank, IT, Education, Engineering, Electrical, Electronic, Textile, Petro, Power, Food and Service industries.

1.    Ultimate Quality Solutions provides trainings on management and industrial modules.

1.    Ultimate Quality Solutions are involved for Development, Implementation and Auditing of Quality systems for ISO 9001, 14001, 22000, 27000, HACCP, OHSAS 18001 etc.

1.    Ultimate Quality Solutions offer WIN-WIN-WIN situation for Organization, Consultant and Customer by

ü Faster Certification

ü Continual Improvement Process

ü Reduced Documentation

ü Better Data Analysis

ü Increased productivity

ü Enhanced staff motivation

ü Competitive advantage

ü More effective use of resources

ü Enhanced customer satisfaction&

1.    Ultimate Quality Solutions systems prevent organization paying “High Cost for Low Quality Data”, which is in consistent irreconcilable, thus saving countless unproductive hours to reconcile them. 

1.    Ultimate Quality Solutions provides value added services for ISO 9001:2015 certifications only to recognitions looking for improvement and is not an agent for ISO Certification.