『One』 What is the process of applying for certification of confidentiality and what conditions need to have
Your question is not comprehensive What is the confidentiality of the qualification certificate ah HACCP certification - that is, "management system certification for processing procedures ", applied only to the food industry, emphasizing the assurance of food safety and hygiene.
Processing Department: Municipal Bureau of Quality and Technical Supervision Quality Management Association
Processing Procedures
(a) Application (intention) Acceptance:
Proposed to apply for certification organization (hereinafter referred to as the guided party) need to apply for the organization to provide a brief description of the organization, the business license, the production process flow charts (service flow, workflow) and other information.
(B) the system to establish and maintain:
1, the organization guided by the party for the initial visit and consultation with the development of certification guidance work plan and schedule;
2, arrange for experts to guide the party to carry out the ISO9000 family, ISO14000 family, GB/T28000 family of standards for training;
3, the organization of the guided by the party to prepare documents for training, guidance system The party to be guided by the document preparation training, guidance system document preparation, review, modification;
4, organization and guidance for the training of internal auditors;
5, in the process of system operation, organization and guidance of internal audits and management reviews, and to assist in the rectification;
6, summing up.
(C) certified:
1, the organization to the national famous certification center to apply for certification;
2, the certification body to send auditors to the guided party review, qualified and issued a certificate.
Processing period: three months from the date of establishment of the system.
Benefits:
1, improve product quality, win the market
Licensing information
1, food production license application (in triplicate, the format text see Annex 1, see Annex 2 for the model text)
2, business license (copy, in triplicate)
3, food hygiene license (copy, in triplicate) (three copies)
4, enterprise code certificate (except for enterprises that do not need to apply for a code certificate. Copy, in triplicate)
5, the person in charge of the enterprise (legal representative) identity card (copy, in triplicate)
6, the layout of the enterprise's production site (a copy)
7, the enterprise's production process flow chart (a copy)
8, the enterprise's quality management documents (a copy)
9, the text of the enterprise standard (the implementation of the enterprise standard) enterprises to provide, a copy)
10, HACCP system certification, export food hygiene registration (registration) certificate (has been obtained by the enterprise to provide. (Copy, in triplicate)
Other information you need to the local "Municipal Quality and Technical Supervision Bureau of Quality Management Association" for more information
Thank you for reading.
『II』 ISO13485 certification need to apply for
1. The applicant organization should have a legal person business license or documents to prove its legal status.
2. has obtained a production license or other special qualification certificate (state or departmental regulations require);
3. apply for certification of the quality management system covered by the product should be in line with relevant national standards, industry standards or registered product standards (enterprise standards), product stereotypes and batch production.
4. The applicant organization should establish a management system in line with the standards to be applied for certification, the production of medical devices, business enterprises should also be consistent with the requirements of the YY/T 0287 standard, the production of three types of medical devices, the quality management system running time of not less than six months, other types of organizations, the quality management system running time of not less than three months.
5. The applicant organization has conducted at least one comprehensive internal audit and one management review.
6. In the year before the application for certification, the applicant organization's products without major customer complaints and quality incidents.
What are the requirements for CMMI certification
CMMI Level 3, known as the Definition Level. At the Definition level, an enterprise can not only have a complete set of management measures for project implementation and ensure the completion of the project; moreover, the enterprise can institutionalize the management system and process according to its own special circumstances and its own standard process, so that the enterprise can not only achieve successful implementation of the same type of project, but also achieve successful implementation of different types of projects. Scientific management has become a culture of the enterprise, the enterprise's organizational wealth. For details, please check the network reference
『肆』 Declare ISO9001 certification need to prepare which documents
ISO9001 system certification needs to prepare a lot of information, the relevant documents will need: 1, quality manual; 2, program documents; back to the 3, third-order documents; 4, management review; 5, internal audit; 6, the program documents in the relevant forms.
In addition, it is also necessary to provide the relevant records of the enterprise, the calibration report of measuring instruments, the documents of the enterprise's internal audit, maintenance and repair of machinery and equipment, and other related records and so on.
Quality manual, procedure documents
Certification application form
Organization profile
Production process, service workflow diagram
Business license, organization code Some also need to qualify
Products and major raw materials used in the national, industry, corporate standards directory
If you still do not understand the You can find me, we are a certification body in Tianjin.
『Wu』 ISO20000 certification need to prepare what information
1, the organization to weave the source of legal documents, such as business license and annual inspection certificate copy;
2, organization code certificate copy;
3, the application for certification system to prove that the effective operation of the document (such as the system document release control table, time-stamped records, etc.);
3, the application for certification system to prove that the effective operation of the document (such as system document release control table, time-stamped records, etc.). Copy);
4, the applicant organization profile; (specific details of the documents can consult the Wuhan Dieshi information technology company professionals)
5, the applicant organization's system documents, (specific contains detailed process conditions please consult the Wuhan Dieshi information technology company professionals)
6, the applicant organization's system documents and the ISO/IEC20000-1: 2005 (E), and the ISO/IEC20000-1: 2005 (E), and the ISO/IEC20000-1: 2005 (E). 2005 (E) requirements of the document against the description;
7, the application of the organization's internal audit and management review of the supporting information;
8, the application of the organization's records confidentiality or sensitivity statement;
『Lu 』 through the ISO27001 certification requirements
Certification has the following materials need to be prepared:
1, the organization of the law Proof of documents, such as business license and a copy of the annual inspection certificate (stamped);
2, a copy of the organization code certificate, a copy of the tax registration certificate (stamped);
3, apply for certification of the organization's information security management system to prove the effective operation of the document (such as the system document release control form, a copy of the time-stamped records, etc.);
4, the application for Introduction to the organization:
(1) Introduction to the organization (about 1,000 words);
(2) The main business processes of the applicant organization;
(3) Organization chart or functional representation of the document;
5, the system documents of the applicant organization, which need to be included, but are not limited to (can be merged):
5.1, the information security management system ISMS policy document;
5.2, risk assessment procedures;
5.3, statement of applicability;
5.4, risk treatment procedures;
5.5, document control procedures;
5.6, record control procedures;
5.7, internal audit procedures;
5.8, management Review Procedures;
5.9, Corrective Action and Preventive Action Procedures;
5.10, Procedures for Measuring the Effectiveness of Controls;
5.11, Functional Role Assignment Sheet;
5.12, Structure and List of Documents for the Entire System.
6, the applicant organization's system documents and GB/T22080-2008/ISO/IEC 27001:2005 requirements of the documents against the description;
7, the applicant organization's internal audit and management review of the supporting information;
8, the applicant organization's records of confidentiality or sensitivity statement;
9, the certification body requires the application for the Other additional information submitted by the organization
For certification, you can refer to the certification information:
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The latest through the certification information, I hope to help you.
『7』 About the auditor's certification exam.
The national registered auditor to be through the CCAA (China Certification and Accreditation Association) organized by the national unified qualification examination, and in accordance with the registration requirements through the certification body for registration, with certain educational requirements, with the provisions of the internship auditor work experience, engaged in certification auditing work of the registered auditor.
Registered auditor categories:
1, quality management system (QMS) nationally registered auditors
2, environmental management system (EMS) nationally registered auditors
3, occupational health and safety management system (OHSMS) nationally registered auditors
4, energy management system (EnMS) nationally registered auditor Auditor
(7) organizations applying for certification should have what conditions extended reading
Auditor's responsibilities:
1, the use of auditing principles, procedures and techniques;
2, effective planning and organization of the work;
3, according to the agreed timetable for the audit;
4. prioritize important issues;
5. gather information through effective interviewing, listening, observation, and review of documents, records, and data;
6. understand the appropriateness and consequences of sampling techniques used in the audit;
7. verify the accuracy of information gathered;
8. confirm the sufficiency and appropriateness of audit evidence to Support audit findings and conclusions.
『High』 How to apply for HACCP certification what qualifications are needed to apply for the certification of what benefits
The question you asked is very difficult for me. I was in my uncle's help, I found the following information for you to choose: HACCP certification - that is, "management system certification for the program", only applied to the food industry, emphasizing the assurance of food safety, hygiene. Processing Department: Municipal Bureau of Quality and Technical Supervision Quality Management Association for the procedure (a) application (intention) acceptance: To apply for certification organization (hereinafter referred to as the guided party) to apply for the organization needs to be provided with a brief description of the organization, business license, the production process flow chart (service flow, workflow) and other information. (B) system establishment, maintenance: 1, the organization guided by the party for the initial visit and consultation with its development of certification guidance work plan and time schedule; 2, arrange for experts to guide the party to ISO9000 family, ISO14000 family, GB/T28000 family and other standards for training; 3, the organization of the party to be guided by the preparation of documents for training to guide the preparation of the system documents, review, modification; 4, Organize and guide the training of internal auditors; 5, in the process of system operation to organize and guide the internal audit and management review, and assist in rectification; 6, summary. (C) certified: 1, the organization to the national famous certification center to apply for certification; 2, the certification body to send auditors to the guided party review, qualified and issued a certificate. Processing period: three months from the date of establishment of the system. Benefits: 1, improve product quality, win the market for certification information 1, food production license application (in triplicate, the format text see Annex 1, the model text see Annex 2) 2, business license (copy, in triplicate) 3, food hygiene license (copy, in triplicate) 4, enterprise code certificate (except for enterprises that do not need to apply for a code certificate. Copy, in triplicate) 5, the person in charge of the enterprise (legal representative) identity card (copy, in triplicate) 6, the layout of the enterprise production site (a) 7, the enterprise production process map (a) 8, the enterprise quality management documents (a) 9, the text of the enterprise standard (the implementation of the enterprise standard for the enterprise to provide, a copy) copy, in triplicate)
『Jiu』 through the iso27001 certification enterprises to have what conditions
Enterprises in the application for iso27001 certification need to provide the following materials:
1 legal status documents (such as business license within the enterprise legal person, business unit legal person code certificates, corporate registration certificate of associations, etc.), organization code certificates;
2 valid qualification certificates, product production licenses mandatory product certification certificates, etc. (
2 valid qualification certificates, product production licenses mandatory product certification certificates, etc.). Compulsory product certification licenses, etc. (when required)
3 Organizational profile (products and products / services related to technical standards, mandatory standards, the use of equipment, personnel, etc.)
4 Application for certification of the production of products, processing or service process flow chart;
5 Temporary premises, multi-premises need to provide a list of;
6 Management Manual, Procedure documents and organizational charts;
7 The number of servers and the number of terminals;
8 Declaration of applicability, list of assets
9 Non-disclosure agreements, statements of information security sensitive areas;
10 Support iso27001 information security management system procedures and control measures, description of the risk assessment methodology, risk assessment report, risk management plan, the organization's efforts to ensure that its information security management system and control measures. Disposition Plan, documented procedures required by the organization to ensure the effective specification/operation and control of its information security processes, and a description of how to measure the effectiveness of controls.
『Pick up』 applying for ISO13485 certification organization needs to prepare what information
1) apply for quality management system certification conditions
1, the applicant should hold the "Medical Device Manufacturer's License" and other qualifications to prove material.
2, the quality system covered by the product should be in line with the provisions of the relevant national standards or industry standards, medical device products should be qualified for registration, the product has been finalized into batch production.
3, the applicant should be based on the standards to be applied for certification according to the establishment of documented management system, and formal operation. Production of three types of medical device products, quality management system operation time shall not be less than 6 months, the production of other products, system operation time of not less than 3 months. And at least two internal audit and a management review.
4, apply for coverage of the product should be normal mass production, to ensure that the normal audit of the production site, and can provide adequate quality records.
5, in the year before the application for certification, the applicant's quality management system covered products without major quality incidents.
(2) The applicant for quality management system certification of the applicant shall submit the following materials
1, the applicant signed by an authorized representative of the quality system certification application;
2, the applicant's business license (a copy);
3, the applicant's quality manual and procedural documents;
4, the product production process and the special process, the key process description;
4, product production process and special process, the key process description;
5, the product covered by the certification application within one year prior to no major quality incidents. Process description;
5, product sales in the past two years and user feedback;
6, product profile and the list of major outsourcing parts, outsourcing parts;
7, "Medical Device Manufacturing License" and "Medical Device Product Registration Certificate" (copy);
8, if applying for product certification at the same time, the same material can be submitted to only one.