Why Should It Be Taken?

ISO 9001 2015 Quality Certificate is obtained by a company, company or organization for the following reasons.

Companies that want to upgrade their Company Management to the requirements of the ISO 9001 Quality Management System Standard, an internationally proven standard.
Companies that want to prove to the customers or other stakeholders of the companies with regular systems that their systems are in International Quality standards.
Companies that want to increase or improve the performance of the Company Quality Management Systems.
Required by customers or Company Partners.
Mandatory by the companies of the company that the supplier is in the position of.
Reasons for requiring the public sector, which is the legal authority, to evaluate companies equally in tenders.

Annex SL

Annex SL is the standard that defines the new top level structure for all ISO management systems standards.

What is EK SL?

Annex SL provides the new high-level structure for ISO management systems standards – replacing the historic ISO Guide and expanding the already implemented base structure.
It was created to introduce the same basic text and common terms and definitions. This will:
Streamlining the standards
Promoting standardization
Facilitating the integration of management systems

PRACTICAL EXAMPLES

Annex SL will only affect future management systems standards – for example, it will not be affected by ISO 9001: 2008, but the new ISO 9001: 2015 will follow the structure, main text and definitions of Annex SL.

Certificates issued by certification bodies accredited by TURKAK (TURKAK ACCRESITATION AGENCY) on Management Systems Certification (ISO 9001: 2015 14001: 2015 ISO 27001, ISO 22000 etc.) will now be published on the TURKAK website. As of April 1, 2017, each document whose application has been audited and certified must have a QR code and Certificate number to be issued by TURKAK. Documents such as ISO 9001: 2015 Quality Management System issued by certification bodies will be published on TDBS (TURKAK CERTIFICATE VERIFICATION SYSTEM).

The certification company that will conduct the audit will inform TURKAK before coming to audit you and will send a separate auditor at that date to CONFIRM the Auditor, System, Documentation and the company. There must be a QR code and Certificate number to be issued by TURKAK. Documents such as ISO 9001: 2015 Quality Management System issued by certification bodies will be published on TDBS (TURKAK CERTIFICATE VERIFICATION SYSTEM).

You can verify your document from the link below.

https://tbds.turkak.org.tr/

Why Should It Be Taken?

Environmental standards, national and international laws, legislation and regulations that we can minimize the damage we cause to the environment on an international scale have been put into practice. The importance of obtaining the ISO 14001 certificate arises at this point. This standard will enable us to have a management system understanding that leads us in the implementation of national and international legislation and helps us to minimize the factors affecting the environment in its activities.

ISO 22000 FOOD SAFETY MANAGEMENT SYSTEM

Undoubtedly, our basic need for our survival is food. Consuming food, which is our most basic need, is an inevitable need.

ISO 22000 is a management system standard that covers the necessary conditions for organizations in the food chain to ensure that food is safe at the time of consumption and to control threats to food safety.

The ISO 22000: 2005 standard published by the International Standard Organization on September 01, 2005 is the first international standard published as a Food Safety management system.

The most important of the basic approaches of the ISO 22000 Standard is HACCP. (Hazard Analysis and Critical Control Points – Hazard Analysis and Critical Control Points) It is a point where control can be applied in order to detect and prevent potential dangers in the food chain, to reduce them to acceptable limits, or to eliminate them.

It has been called the Supply Chain Security Management System, and in many sectors, breaks or security problems that may arise in the rings of the supply chain negatively affect organizations. It is of great importance for such organizations to determine the risks related to the supply chain correctly and to manage these risks effectively.

The Supply Chain Security Management System is an international standard, it defines the requirements of the Supply Chain Security Management System and provides a management model for organizations that want to implement this system. The organization’s activities related to supply chain security are ISO 9001, ISO 14001, ISO 22000, ISO 27001 etc. It wants to ensure the effective management of supply chain risks by integrating it with management systems such as.

The Supply Chain Security Management System can be purchased by anyone from organizations of all sizes, to global organizations of international size, from factories, to companies that provide service storage or transportation services, to companies at any stage of the supply chain.

The European Data Protection Board (European Data Protection Board) includes the EDPB, as well as the ISO 27701 standard with the feedback and suggestions of 25 different institutions and organizations; ISO (SC 27) was developed by the information security, cyber security and privacy protection committee.

The ISO / IEC 27701: 2019 standard is from the ISO 27000 Information Security Management Systems Standards family and was prepared by the ISO / IEC JTC1 / SC27 Information security, cyber security and privacy protection technical committee and published on August 6, 2019.

ISO 37001: 2016 specifies and guides the requirements for the establishment, implementation, maintenance, review and development of an anti-corruption management system. The system can be stand-alone or integrated into a general management system. ISO 37001: 2016 addresses the following in relation to the organization’s activities:

Corruption in the public, private and non-profit sectors;
Corruption by the organization;
Corruption by staff working on behalf of the organization or by the beneficiary organization;
Corruption by the organization’s business partners acting on behalf of the organization or for its benefit;
Bribery of the organization;
Corruption of the organization’s staff in relation to the organization’s activities;
Corruption related to the organization’s activities in relation to the organization’s business partners;
Direct and indirect corruption (For example, corruption proposed or accepted by or through a third party).

ISO 37001: 2016 is only valid for corruption. It sets and guides the requirements for a management system designed to help an organization prevent, detect and respond to corruption and comply with anti-corruption laws and voluntary commitments applicable to its activities.

While ISO 37001: 2016 does not specifically address fraud, cartel and other anti-trust / competition offenses, money laundering, or other activities related to corruption, an organization may choose to expand the scope of its management system to include such activities.

The requirements of ISO 37001: 2016 are generic and can be applied to all organizations (or parts of an organization), regardless of the type, size and nature of the activity and whether in the public, private or non-profit sectors.

One of the processes that organizations should manage effectively is business continuity. Business continuity; It is defined as “the capacity of an organization to maintain its products and services at a predefined acceptable level after an outage event”. In other words, it is all the activities that will enable all businesses, large or small, to respond to the disruptions that cause their business to disrupt. If unexpected business interruptions are not for you, the best thing to do is to apply the ISO 22301 Social Security and Business Continuity Management System Standard.

ISO 22301 Social Security and Business Continuity Management System Standard is a standard approved by approximately 160 countries and is an advanced application of the previously published BS 25999 Business Continuity Standard, which was issued as an ISO standard.

The ISO 22301 Standard specifies the requirements for organizations to create the necessary plans to ensure business continuity, to implement, monitor, review, maintain, protect and prepare to reduce risks, to develop a documented management system to recover from catastrophic events.

What are the Benefits of ISO 22301 Social Security and Business Continuity Management System?

It contributes to identifying current and future business threats and managing them correctly.
It minimizes the impact of events.
It ensures that critical functions always work in times of crisis.
Provides an advantage in today’s competitive environment by proving its ability to ensure its continuity.
The requirements of suppliers, customers, shareholders and employees are fulfilled through risk assessment.
It provides reduction of downtime and improvement of recovery time in the face of events.
Recognition of the organization itself and other affiliated entities, public institutions, local authorities and a properly developed, documented and understood emergency service is provided.
It protects the organization’s reputation, brands and reputation.
The organization’s supply chain becomes secure.

The Quality Management System (ISO) gathers the rules that companies working in different fields must comply with under various headings. Although the systems are generally based on the ISO 9001 system, it may appear as a different standard when separated in some places. Developed for the Quality Management System of Medical Devices, ISO 13485 is a quality management system with special conditions for medical devices. Companies that manufacture, sell, provide services or raw materials, carry out warehouse activities, and provide technical service and maintenance services in the field of medical devices must act in accordance with the specified quality management system requirements. These conditions, which have been applied for a long time throughout the world, are also applied to companies serving in our country. In other words, if a company provides production, sales, service or raw material supply, warehouse service, technical support and maintenance and repair services related to medical devices, it has to apply ISO13485 requirements.

An effective Occupational Health and Safety Management System will help you protect your most valuable asset, your employees, and enable you to achieve business excellence.

ISO 45001: 2018 will provide you with the following benefits;

Increased organizational resilience through proactive risk prevention and continuous improvement of O&S performance
• Strengthening legal and regulatory compliance
• Prove your social responsibility awareness by showing your commitment to safe, healthy and sustainable work.
• Creating a better working environment for your employees and minimizing occupational accidents
• Protecting your brand and corporate reputation

Since the SO 14001 Environmental Management System Standard and the related standards series are in compliance with the environmental laws and regulations for implementation in all countries as of their preparation, the practices are generally in parallel with the fulfillment of the obligations brought by the legislative requirements and form the basis for the implementation of the practices within a system. . The ISO 14000 standard series includes many standards. The most important and known of these standards are:

ISO 14001 Environmental Management Systems – Terms and User Guide
ISO 14004 Environmental Management Systems – General Guide on Principles, Systems and Supporting Techniques
ISO 14020 Environmental Labels and Declarations – General Principles
ISO 14031 Environmental Management – Environmental Performance Assessment – Guide
ISO 14040 Environmental Management – Lifelong Assessment – Principles and Framework

As a result;

The ISO 14001 Standard is a standard created to minimize the damage to the environment.
ISO 14001 practices are generally in parallel with meeting legislative obligations.
ISO 14001 is not a product standard, it deals with how it is produced, not what is produced.
It is a voluntary management system that can be applied to any business regardless of sector and scale.

What are the Benefits of ISO 14001 Environmental Management System?

Compliance with national and international legal regulations.
It facilitates obtaining permits and authorization documents.
Provides national and international reputation.
Costs arising from environmental effects are reduced.
As a result of the effective use of natural resources, costs decrease and productivity increases.
Customer confidence increases by assuring the customer that an obligation to environmental management is undertaken.
It reduces incidents that result in liability, thus providing the potential to lower liability insurance costs.
Pollution arising from company activities is taken under control starting from the source and pollution is reduced.
Due to the identification of potential danger situations, there is a decrease in the incidents resulting in loss due to the preparedness for emergencies and accidents.
Workplace quality and thus worker morale are increased and commitment to the business increases.
Thanks to the trainings given to the personnel, the environmental awareness of the employees is increased.
It makes it easier to enter markets where green production processes are important.

SA 8000 is a standard that takes the ISO 9001 Quality Management System Standard and ISO 14001 Environmental Management System Standard as an example, cares about the procedures and system conditions as well as the performance conditions, and the combination of management system and behavior code is a standard.

ISO 27001 certification is an iso document that helps organizations keep and manage their and their customers’ confidential information safe.

ISO 27001 Information Security Management System is an international framework that helps companies protect their financial data, intellectual property, and sensitive customer information. With ISO 27001, companies can identify their risks, manage or reduce the risks of confidential information. In addition, they fulfill the necessary security measures in this direction. This helps you to continually refine and refine your methods, not only today but also for the future. ISO 27001 protects the reputation of your business and your company reputation. It adds value to your business by giving confidence to your customers and all your stakeholders.

Two standards related to the AS 9100 series standards, which are prepared by the International Quality Group Aerospace Industries and can be applied to all enterprises that design and manufacture various parts and components for the aviation and space industry, draw attention. One of these is the AS 9110 standard for suppliers that provide repair and maintenance services. The other is the AS 9120 standard for distributors.

Why Should It Be Taken?

It is a Quality Management System Standard developed by the International Quality Group Aerospace Industries. Although based on ISO 9001, it includes Appendices, Tasks, Responsibilities and comments specific to the Aerospace and Defense industries. Do not forget that in this sector, there will be special requests from your suppliers, suppliers and customers and you are obliged to make them, to implement and to show them. It is a unique and high-level QUALITY SYSTEM.

– Integrated System Setup
– What are the External and Internal (in Context) issues of the company.
– What are their Titles and Purposes.
– What is the strategy, how will its applications be.
– Are there any plans to reach them.
– What is the intended result of the QMS.
– How is this internal and external issue monitored and analyzed, what are the consequences.
– If these internal and external issues are relevant, what are their needs?
– How do you make an international application?
– Products and Services are affected by these.
– How top management’s commitment is formed.
– Who and how decides whether the resources used for these are suitable for use.
– Production Planning Meeting and Production Stages
– Organization structure suitability and (OEK) Organization manual
– Organization Chart determined in accordance with management
– (FAI) Transactions
– Determination of Process and Processes interaction scheme
– Process (Process) Audits
– Measurement of Process and Process, Data Analysis
– Determining the owners of the processes and processes and their follow-up in accordance with the process cards
– Preparation of Annual Training, Internal Audit, Process, Configuration plans for the company.
– Follow-up of ISG Training plans
– Approval of External Suppliers for the preparation of Audit plans
– Job scheduling Man Hour management and Tracking
– Internal Audit (Internal) Audits
– 3rd Party Supplier Audits and Question List Preparation
– Control of the work done outside the supplier premises,
– Documentation Revision and Renewal follow-up list
– Control of Records, Tracking and Archiving
– Customer property
– Revision follow-up notification of external documents and approval by the customer
– Reviewing Mission, Vision, Values
– Determination and follow-up of Quality, Safety and Environmental Policies
– Inputs and outputs of YGG Meetings, implementation and follow-up
– Identification, tracking and implementation of the Labels used in the system
– Internal Audit and Process Audit Question Preparation
– Configuration Management,
– Implementing changes Identifying critical personnel
– Proxy System and Working Methods
– Customer Ownership and requirements
– Internal and External Communication Establishment and Requirements
– Design, design verification and testing process,
– Training of relevant personnel for understanding customer documents.
Reliability and sustainability
– Supplier approval,
– Verification of purchased products,
– Review of Tender and Bid Requests
– Transferred Jobs
– Computing and Information Security
– Administrative Affairs and Human Resources
– Personnel Responsibility and Evaluation
– Seal and signature authorization chart
– Personnel responsibilities and Critical Personnel
Traceability throughout the life of the product,
– Product documentation,
– Preparation of Work Orders
– Understanding of POs and approval of follow-up of necessary transactions
– Control of manufacturing process changes,
– Control of manufacturing equipment and tools and CNC programs,
– Special processes,
– Outsourced Processes
Traceability
– Measuring Processes
– Determination of targets and compliance with the Policy
– Inspection and test processes,
– Calibration Verification and Procedures.
– Implementation of maintenance plans (for each device) follow-up and up-to-dateness
– Leadership and the purpose of Leader Management.
– Common area usage or used programs authorization matrix (such as ERP)
– Risk-based thinking and implementation systems
– Risk identification, reduction and residual risks
– Risk Management
– Evaluation of Danger Events
– Accident Margin (Near Miss Incident) notifications
– Areas with ESD and Control Programs
– Establishing a suggestion system, Follow-up Management and Evaluation
– Methods, resources and records,
– Determination of Resources in processes and processes
– Staff Orientation and recurrent refresher training plan and follow-up.
– Warehouse Stock Control Working and Methods warehouse layout.
– Determining the appropriate material storage and location for the customer
– Scrap operations (HEK) separated material warehouse keeping documents and documentation
– First entry checks of purchased or customer-brought materials
– Follow-up of interim controls at the appropriate place and in accordance with customer requests
– Final control and product delivery.
– Transport, Shipment, Packaging and Packaging methods
– Project Preparation, Project Management Tracking
– Review of Demand, Offer, Tenders and Contracts, Assessment
– Things to do in case of returns and non-conformities from the customer
– Transactions that need to be followed up for errors and nonconformities
– ROOT CAUSE ANALYSIS for Urgent (CAPA) s in order not to repeat it again
Corrective measures,
– Internal Audit requirements,
– Choosing internal auditors or getting service by contracting
– First part inspection (FAI),
– Disposal of unsuitable product,
– The first product (raw material) entering the system