GOST R Certification Process

Before starting to GOST R Certification process you have to understand what is GOST R Certification,

GOST R known as GOvernment STandard Russia. GOST R standard was delivered by the government of the Soviet Union as a major aspect of its national standardization system and later embraced by the CIS. GOST R declaration requires overseeing exchange Russia. GOST R also called as identification for your merchandise required in Russia. GOST R is the legitimate quality certification framework in Russian Federation. In different words, it is called as GOST-R Certification. GOST R certification is mandatory for a wide scope of items.

GOST R certification is planned to give security and high caliber of items and administrations to customers. This privilege of the Customer for security and quality is ensured by the required accreditation of local as well as also outside produce. Produce that enters the region of the Russian Federation and that is liable to compulsory affirmation as indicated by the enactment of the Russian Federation must meet the prerequisites of Russian accreditation framework. The certificate can be substantial for a one-time-just shipment or for a time of 1 or 3 years.

GOST-R Certificate is required for use at

• Products sold in retail
• Places like industrial kitchens or laundries (to obtain an Operational License)
• Production Facilities and Factories (to obtain a Work and Production Permit)
• Constructions (to obtain an inhabitation license)
• Russian Federation and Belarus customs (compulsory)

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Does GOST R Certification is Necessary?

Normally, Certificate is essential for:

• Customs house
• Selling and using at the Russian market

The certification procedure for items and administrations may be mandatory or intentional. Accreditation framework had been made to ensure Consumer's privileges and dodge the import of low-quality items. Affirmation law builds up principles and standards which must be met to get GOST-R certificate. There are likewise guidelines saying which items are subjects to required accreditation and which may have an intentional declaration.

As per the goals of the State Customs Committee of Russia from 01.10.2000, generation of outside producers brought into FR should fulfill the national quality guidelines, in this way is a subject to confirmation. Confirmation GOST R relates to determined items or modern action of the organization. Declarations are issued on a base of ability results, so items which very much experienced the confirmation procedure have no troubles while enlisting at customs.

All the above data demonstrates why Russian organizations and companies can't work with items with didn't get GOST-R certificate.

Benefits of GOST R Certification

• Customer wellbeing.
• It helps to enhance brand image and market value of the company.
• Supports to reach the Russian market easily.
• Customer fulfillment.
• Money-saving and time-saving process.
• The reputation of an association increment.
• Limits hazard.
• It helps to acquire the Russian market.
• Counteracts Wastage of assets.
• Saves cost.
• Permit to exchange the Russian market.
• Opens another market for the business.
• It helps to reduce the hazard, deserted items, and harms.
• The advantage of International stature to your item.
• Better Retailing opportunity in Russia.
• Encouragement of foreign trade.

Requirements of GOST R Certification

• Conduct Product testing
• Scrutiny of requirements
• Application for certificate
• Carry out inspection
• Verify product safety and quality
• Evaluation of the product
• Take enforcement actions
• Make quality enhancement, if required
• Internal audit
• Testing of products and safety
• Classification of requirements

What documents are needed to estimate cost and terms for a GOST R Russia certification?

The initial step while in transit to GOST R certification is to see precisely how Russian law or the EAC guideline characterizes creation, which is the reason there are four things of data required:

• Name of the product
• Customs Product Code
• Brief description of the product
• Manufacturer declaration of conformity
• Samples of the product (if necessary)
• Later on, in the event that you choose to continue with GOST certification, an ISO declaration of congruity ISO or a CE Marking of your item might be required, yet just in a couple of uncommon cases.

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GOST R Certification Process

These declarations are given by the Certification Organs which is licensed by "The Federal Agency on Technical Regulating and Metrology".
To make the GOST R Certification process simple. You should hire a consultant when a consultant received your application they will guide you and your business through the following steps.

• Testing
• Documentation & Test Report
• Process Audit
• The procedure of Production Analyses

For the greater part of the items, a few examples will be sent to Moscow for the vital test as per the Russian standards.

• Certification and beyond 

BIFMA Certification and Consultant

BIFMA stands for Business and Institutional Furniture Manufacturer’s Association, BIFMA was established in 1973, BIFMA certification is the not‐for-profit trade association for business and institutional furniture manufacturers. BIFMA certification focuses on developing, designing and marketing of office and institutional furniture products.

BIFMA is also authorized by ANSI to be the director of the U.S. Technical Advisory Group to ISO Technical Committee TC-136 Furniture. This has been so helpful for BIFMA in its engagement with International Standards for office furniture. However, ISO TC-136 covers ALL furniture. Those who are interested in International Standards for furniture another than office furniture they should obtain BIFMA certification. There are over 1,200 ANSI-authorized standards set in place that are created to protect customers, the workforce as a quantity and the common public. ANSI is responsible for the first American Standard Safety Code, published in 1921, which showed the value of both head security and eye protection for industrial workers.

BIFMA certification provides healthy, productive and comfortable workspaces – rests on a base of engineering and materials standards architects, interior designers, facility managers, and other overall industries with an easy process to identify frequently sustainable products. BIFMA provides a competing advantage of building performance criteria that focuses on the improvement of environmental and social aspects through the supply chain.

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BIFMA Product Safety and Performance Standards and Guidelines

• ANSI/BIFMA X5.1 Office Seating
• ANSI/BIFMA X5.4 Lounge and Public Seating
• ANSI/BIFMA X6.4 Occasional-Use Seating
• ANSI/BIFMA X5.5 Desk Products
• ANSI/BIFMA X5.6 Panel Systems
• ANSI/BIFMA X5.9 Storage
• ANSI/BIFMA X5.11 Large Occupant Office Seating
• ANSI/BIFMA X6.1 Educational Seating
• ANSI/SOHO S6.5 Small Office/Home Office
• ANSI/BIFMA M7.1 Standard Test Method for Determining VOC Emissions
• ANSI/BIFMA X7.1 Standard for Formaldehyde and TVOC Emissions
• ANSI/BIFMA e3 Furniture Sustainability Standard
• BIFMA HCF 8.1 - Healthcare Furniture Design - Guidelines for Cleanability
• BIFMA G1 - 2013 Ergonomics Guideline for Furniture
• BIFMA Color - 2005 Color Measurement
• BIFMA PCR for Office Furniture Workspace Products: UNCPC3814
• BIFMA PCR for Seating: UNCPC 3811
• BIFMA PCR for Storage: UNCPC 3812
• BIFMA PD-1-2017 Mechanical Test Standards-Compiled Definitions
• BIFMA Sustainability Guidelines for Office Furniture - 2005
• BIFMA Tex4.1 - 2005 Woven Textile Characteristics

Benefits of BIFMA Certification

There are some advantages to buying BIFMA approved furniture. There is insurance that any BIFMA-authorized furniture has met harsh standards for safety. You can feel positive in the fact that any piece of BIFMA-approved furniture will help promote a working environment that is practical and healthy.

• BIFMA products enhance a healthful work environment, which can boost productivity and reduce work-related injuries.
• Helps your internal sustainable management objectives.
• Customers and shareholders have confidence & trust in you.
• Establishes your management credentials in the office furniture industry.
• Establishes a path for constant improvement.
• Helps you meet state and federal procurement necessities.
• Most BIFMA certified products carry a warranty of 5 years or longer.
• BIFMA certificate provides assurance and preference to your customers and stakeholders on the economic, social and environmental standard of the products.
• Your product is certified to meet the International standard of furniture products quality maintenance and development.
• There is an ongoing improvement in your organization.
• Anticipate risks and opportunities.
• Product quality is improved to meet BIFMA requirements.
• Mandates continuous monitoring & measurement of the processes that prevent unintended derailments.
• BIFMA certification ensures a durable and long-lasting product that will last many years.

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How To Get BIFMA Certification

To make the BIFMA Certification process simple. You should hire a consultant when a consultant received your application they will guide you and your business through the following steps.

• Gap analysis 
• Formal assessment 
• Training
• Documentation
• Internal Audit
• External Audit
• BIFMA Plan & how to get Certified
• Certification and beyond 

How to get HACCP Certification

The HACCP stands for Hazard analysis and critical control points. HACCP is basically a tool to help recognize and control food safety hazards that may occur in the food business. (Physical Hazards, Chemical Hazards & Biological Hazards) The HACCP system can be used at all stages of a food chain to all big, small, suppliers, manufacturers, trading, supply, Enterprises, retailers, transportation, packing farming, etc of a food product. A HACCP system permits you to recognize hazards and fixed in place controls to manage these during your supply chain while production. The HACCP system satisfies the requirements of the Codex Alimentarius Commission (CAC) – which produced by the World Health Organization and the Food and Agriculture Organization of the United Nations to make together worldwide food standards, guidelines, and codes of practice to assure fair trade.

By implementing a HACCP Certification It helps to reduce the likelihood of customer complaints or a recall by identifying and controlling potential hazards which may come from raw materials, facility processes, and human error, The Prevention from diseases and chemical hazards, Implement an internationally recognized food safety system, It also analyze and improve your system so it stays active. The more excellent employee awareness that results from a HACCP program serves to drive constant improvement of a company’s products and processes.

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HACCP Principle

As per Codex Alimentarius Commission guidelines, there are seven HACCP principles as given below

• Principle 1 - Conduct a hazard analysis.
• Principle 2 - Determine the critical control points (CCPs).
• Principle 3 - Establish critical limit(s).
• Principle 4 - Establish a system to monitor control of the CCP.
• Principle 5 - Establish the corrective action to be taken when monitoring indicates that a particular CCP is not under control.
• Principle 6 - Establish procedures for verification to confirm that the HACCP system is working effectively.
• Principle 7 - Establish documentation concerning all procedures and records appropriate to these principles and their application.

The 12 steps of HACCP

1. Create a food safety team.
2. Describe the food in great detail.
3. Describe the intended consumer and how they are going to consume the food.
4. Construct a Flow Diagram to Describe the Process.
5. On-site verification of flow diagram.
6. Conduct a hazard analysis.
7. Determine critical control points.
8. Set critical limits of each CCP.
9. Establish a monitoring system for each CCP.
10. Establish corrective action.
11. Verify, then validate.
12. Establish good record keeping and documentation.

Reason to obtain HACCP Certification

HACCP Certificate is outlined to provide an accurate understanding of food safety and HACCP for people with a limited food science or industry experience. It will be of benefit to those wishing to enhance their food safety awareness and will help those with new job responsibilities, new positions or those looking to change careers.

How long does a HACCP Certification audit take?

The Certificate program consists of 3 stages, for a total of 19 modules. well, It really depends on the rules that apply to the type of certification you are trying to achieve and also the physical size of the food business. Food HACCP audits can take anywhere between 1 day and 5 days. Again, it all depends on the audit scope.

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How to get HACCP Certification

To achieve HACCP certification by a reliable HACCP certification provider, the food business is required to sustain an audit or appraisal of its food safety and HACCP policies and methods. This assessment is required to be initiated by competent and qualified food safety auditor.
To make the HACCP certification process simple. You should hire a consultant when a consultant received your application they appoint a client manager who will guide you and your business through the following steps.

• Gap analysis 
• Formal assessment 
• Certification and beyond 
• HACCP Plan & how to get Certified

Why Companies Obtain ISO Certification

You must be wondering whether its worth to obtain ISO certifications for your Company, your Organization, and your business According to dozens of studies, the answer is yes!

Nowadays every company wants to obtain ISO Certification to continuously satisfying customers, management and employees, also to reducing cost and to improve the process. Businesses, irrespective of their size, a business model can get ISO Certification. There are numerous benefits of getting ISO certificate for companies and that is why almost every company thinks they must have ISO Certificate.

Now first you have to understand what is ISO. ISO Standards are a series of the framework that assists you to maintain/run your business successfully/smoothly. ISO certification is verification from an outsider, for example, ourselves, that you comply with an ISO standard. ISO certification gives your association believability. When any company or organizations get certified with ISO it means that there product and services meet the international quality standard. The ISO certification is a lawful or contractual requirement. ISO certification standards are a series of structures that help you to run your business productively. ISO Certificate is evidence from the third party, such as individually, that you follow with an ISO management standard. Customers and stakeholders also start trusting you more. it will also prepare yourself systematically in advanced to handle any critical situation occur in business. Certification adds the reliability of international growth, against other companies that do not express such third-party approvals.

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There are thousands of ISO Certifications are there like most popular ISO 9001, ISO 14001, ISO 27001, etc. Now the company needs to understand which certificate they need. if the organization is about the education they can Obtain ISO 29990, if an organization is in the IT field then they can get ISO 27001. ISO 9001 Certification can be obtained by any company irrespective of its size and shape. Obtaining ISO Certification from genuine ISO Certification Company or from ISO Certification Consultant is very important. There are a lot of fraud companies in the market who provide duplicate certification at very cheap prices. And sometimes big companies didn't do enough research about that certification providers company and end up getting a duplicate certificate. So before hiring any consultant or company to obtain ISO certification, understand their knowledge and how they work and tell them to show their previous work.

Benefits by obtaining ISO Certification

• Increased Credibility and Recognition.
• ISO Certification Helps you become more productive.
• Consumer safety and satisfaction.
• Improving system and process efficiency.
• Improve revenues.
• Empowered Employees.
• Boost your ROI (Return On Investment).
• Opens doors to new markets.
• Applies to all sizes.
• Improved participation of employees.
• Suppliers become more like partners.
• Assures that an organization’s information is secure.
• Makes a strong relationship with your supplier.
• Makes an image as an authority on the quality management process.
• Better perception of your company.

How To Get ISO Certified

The ISO Certification did not certify the organization by itself to get ISO Certification you can contact the third-party that will audit your organization and they will decide that your products processes and services fulfill the ISO Criteria or not. The cost of obtaining ISO certification depends on the size of your company and the Standard you choose. ISO is suitable to all big small suppliers, manufacturers, Enterprises, retailer’s food chain all types of business and any organization.

Also, check ——>> ISO Consultant In Saudi Arabia

To make the ISO certification process more simple. You should hire a consultant when a consultant received your application they appoint a client manager who will guide you and your business through the following steps.

• Gap analysis 
• Formal assessment 
• Certification and beyond 
• ISO Plan & how to get Certified

What Is ISO 13485 Certification

ISO 13485 stands for Medical devices -- Quality management systems Requirements for regulative purposes is an International Organization for Standardization. ISO 13485 was first announced in 1996 and the current standard was published on 1 March 2016. The latest version has a higher accent on risk management and risk-based decision making, as well as differences related to the enhanced regulatory requirements for companies in the supply chain.

ISO 13485 describes the specifications for a complete quality management system for the design and manufacture of medical devices and the organizations involved in the medical device industry. ISO 13485:2016 can be applied by external and internal parties, such as certification bodies, to support them including their auditing manners. The medical profession is observing continuous improvement in its technologies and equipment. It is also essential for the world to ensure safety measures for it.

Benefits Of ISO 13485

• Improve customer satisfaction
• ISO 13485 allows the establishment of the Quality management system in medical device production, life-cycle process, and maintenance.
• Improve the process of production and maintenance of medical devices.
• Enhances the effectiveness of medical devices
• Improve your processes
• Ensures safety in medical devices.
• Reduces operational cost.
• Improve decision-making.
• Continuous Development in medical devices
• Better employee engagement
• Natural trust in stakeholders and consumers
• Validate customer fulfillment and well-being.
• Encouragement of staff and employee training in medical service providers.
• Improve your company’s credibility and image
• Create a culture of continual improvement

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Requirements Of ISO 13485

ISO 13485:2016 defines requirements for a quality management system where an organization needs to demonstrate its capacity to provide medical devices and similar services that consistently meet consumer and managerial requirements.

• Define adequate quality of design and development plan for medical devices.
• Identification of Quality management process in medical device production and further process.
• Consider customer’s requirements throughout the process.
• Production of sterile medical devices.
• Proper maintenance, control, and repair of medical devices.
• Review the quality of design and development in medical devices.
• Meet documentation requirements fundamental to ISO 13485.
• Safe distribution of medical devices.
• An internal audit of the organization.

Who Can Apply ISO 13485?

ISO 13485 can be implemented by any size of medical co-operation provider during the life-cycle of the device. It is entitled in every stage of device life, from planning, production, supply, distribution, storage, installation, controlling, monitoring, maintain and even for post-production.
It is currently applied by the organization in 21 countries. ISO has adopted a process plan which serves the PDCA act (Plan – Do – Check – Act) cycle which begins in a drive for continued fulfillment in the process of the organization. The Organizations connected to one or various steps of a Medical Device Life-cycle or a Supplier or other External Parties giving such organizations with products for example.

Organizations involved in one or more stages of the medical device life-cycle	Suppliers or External Parties who provide products to such Organizations
·         Design and Development	·         Raw materials
·         Production	·         Components
·         Storage	·         Sub-assemblies
·         Distribution	·         Medical devices
·         Installation	·         Sterilization services
·         Servicing	·         Calibration services
	·         Distribution services
	·         Maintenance services

How To Get ISO 13485

6 steps to achieve ISO 13485:2016 certification

• Planning the quality system
• Meeting regulatory requirements
• Implementing design controls
• Documents, records, and training
• Management processes
• The Certification audit

To make the ISO 13485 Certification process simple. You should hire a consultant when a consultant received your application they appoint a client manager who will guide you and your business through the following steps.

• Gap analysis 
• Formal assessment 
• Certification and beyond 
• ISO 13485 Plan & how to get Certified