Monday, 15 April 2019

Top 8 Most Popular ISO Standards

There are lots of ISO standards, sometimes it is difficult to understand that which one is best suitable for your organization. Some ISO standards are generic and used to implement in any organization no matter what type of organization is that, while some of the ISO standards are industry specific. If you are not yet implemented any ISO standard and want to certified or implemented your organization with ISO standard then we are discussing top 8 most popular ISO standards, please read here and prepare your mind to get ISO certification for your organization.

ISO 9001

ISO 9001 is International Quality Standard for Quality Management System (QMS), It was initially created in 1987, than 1994, 2000, 2008 and now 2015 is the most recent adaptation. ISO 9001:2015 standard is bland and actualize in any sort of nature, area, process & size organizations its is exceptionally mainstream standard with 95% of execute in entire associations in the world even numerous nations government make administrative prerequisites for their particular nation associations, India is one of them.

ISO 14001

ISO 14001:1996 was first form of EMS, then ISO 14001:2004 & following eleven years ISO upgrade new form is ISO 14001:2015, now it is most recent variant of EMS.

ISO 14001:2015 is used to enhance the environmental performance of the organization. It will specifies the requirement for the environmental management system. ISO 14001:2015 is used by the organization to manage the environmental responsibilities in systematic manner.

ISO 14001:2015 help the organization to achieve the goal of the environmental management systems, it will provide value for the environment, to the organization itself and interested parties. It will consistent with the environmental policy of the organization.

ISO 20000

ISO/IEC 20000 is a global IT standard that permits organizations to exhibit greatness and demonstrate best practice in IT administration. The standard guarantees organizations can accomplish proof based benchmarks to ceaselessly enhance their conveyance of IT administrations. The selection of ISO/IEC 20000 has developed quickly in the universal coliseum of IT administration suppliers and it has turned into a focused differentiator for conveyance of IT administrations. ISO/IEC 20000 is adjusted to and corresponding to the procedure methodology characterized inside ITIL from the Office of Government Commerce (OGC).

ISO 22000

ISO 22000 is a food safety management system that can be applied to any organization which belongs to food chain industry. If your organization ISO 22000 certified that means your organization have food safety management system in place. This provide the confidence to the customer on your product. Customer demands safe and healthy food and food processors require that ingredient obtained from their supplier to be safe and healthy for their customers.

ISO 27000

ISO/IEC 27001 is specification of information security management system (ISMS). ISO/IEC 27001 formally indicates an administration framework that is planned to bring data security under express administration control. Being a formal determination implies that it commands particular prerequisites. Associations that case to have embraced ISO/IEC 27001 can along these lines be formally evaluated and ensured consistent with the standard.

ISO 13485

ISO 13485 is recently published in 2016, that speaks to the prerequisites of a thorough administration framework for the outline and production of therapeutic gadgets. Standard supersedes prior reports, for example, EN 46001 and EN 46002 (both 1997), the ISO 13485 distributed in 1996 and ISO 13488 (additionally 1996).

The essential goal of ISO 13485 was to encourage blended restorative gadget administrative prerequisites for quality administration frameworks. ISO 13485 is a standalone standard. It is generally focused around the structure of ISO 9001, however incorporates some specific prerequisites for medicinal gadgets, for example, hazard dissection, sterile assembling and trace ability.

ISO 29990

ISO 29990 label essential prerequisites for suppliers of taking in administrations in non-formal training and preparing, will likewise upgrade transparency and permit examination on an overall premise of taking in administrations, offering a solitary option upheld by worldwide agreement to the enormous assortment of national administration and administration benchmarks which now exists in the field of non-formal taking in.

Information is turning into a key component in fruitful corporate administration everywhere throughout the world and training is progressively being viewed as a business-arranged administration.

The goal of ISO 29990 is to give a non specific model to quality proficient practice and execution, and a typical reference for learning service providers (LSPs) and their customers in the configuration, advancement and conveyance of non-formal training, preparing and improvement.

ISO 50000

ISO 50001 is the International Standard for Energy Management System (Enms), discharged in June 2011 that replaces the British and European Standard BS EN 16001:2009.

Energy proficiency and vitality asset administration is exceptionally significant in today's setting of an unnatural weather change and environmental change. Vitality creation is answerable for sixty percent of the planets Green House Gas outflows. The proposed standard is in accordance with this necessity to help firms and associations address and reference vitality administration issues on a worldwide standard.

Sunday, 7 April 2019

Top 5 Reasons To Work With An ISO 9001 Registered Company

Picking an ISO 9001 certified organization offers numerous advantages to you and your organization, however we've quite recently recorded the best five which are listed below:

1. Standardization
     -- ISO 9001 blueprints the criteria for an association's quality management system, which drives standardization. Standardization results in a quality item each time that meets the required particulars; clients can expect the equivalent remarkable items and services without fail.

2. On-time delivery
     -- With standardization comes proficiency, bringing about on-time delivery of items and services. An ISO certified organization as of now has forms set up to ascertain lead times and facilitate each progression in the process from the underlying request to the delivery of the item. These system and associations with believed delivering organizations result in less startling deferrals.

3. Cost reduction
     -- ISO 9001 helps the organizations to constantly reduce the waste and operate more efficiently to deliver more value to customers.

4. Reliability
     -- Having Quality Management System in place results reliable products, and reduce the chance of failure compare to those who don't have an QMS in placed. ISO 9001 certified company already has a set of process to identify and deal with the failures.

5. Customer Satisfaction
     -- Each of the above reasons help to increase the customer satisfaction, the guiding principles of ISO is to ensure the quality of products and services being offered is consistently improves and meets the customer requirements.

What can’t you do with ISO?

You can utilize the way that your organization is ISO 9001:2015 certified in your marketing. Your management system and its procedures have been ensured to ISO 9001 so you would like to discuss your fruitful enlistment to ISO 9001 similarly as long as you don't propose that your items are confirmed or that you are certified by ISO, which is the thing that ISO certified suggests.

What can’t you do with ISO?

  • ISO is a brand and intellectual property, So you can't use or modify ISO logo.
  • You can not say ISO 9001 certified or ISO certified, You must spell it out as -- we are ISO 9001:2015 certified.
  • You can not be use ISO 9001:2015 on your products or used in literature to imply product certification because it is not a product certification It's a company certification.
  • You should be cautious with your scope so it legitimately delineates your confirmed activities and geographic areas.

10 ways an ISO certification can help your business

When we talk about helping organizations acquire ISO 9001:2015 registration, individuals regularly ask us, "For what reason does our organization should be ISO 9001 certified?" Good inquiry. ISO 9001 is the quality management system (QMS) standard and it creates various advantages for any organization willing to go that course. Anyway, for what reason should your association acquire ISO 9001 registration?

Becoming ISO 9001 certified means your organization have to pass a physical audit for ISO 9001:2015 certification from the side of certification body.

Top 10 reasons an ISO certification can help your business:

1. Improve the quality of management system.
2. Get business from new customer and increase the revenue.
3. Meet customer requirements.
4. Increase customer satisfaction.
5. Improve the consistency in the operations.
6. Focus on management and employee.
7. Reduce waste, Improve efficiency and save money.
8. Achieve international quality standard.
9. Improve professional culture in your organization.
10. Easily understand, describe and communicate your company process.

Friday, 29 March 2019

Best ISO Certification Company in india

Some of the Best ISO Certification Bodies in India include the following:-

  • Bureau Veritas
  • Tuv Nord
  • Tuv Sud
  • BSI
  • Tuv Rheinland
  • Intertek
  • URS India
These are the some well known and well establish certification body in India which are working around the globe.

Friday, 9 November 2018

Quality Manual in ISO 9001:2015

QUALITY MANUAL importance in 9001:2015

Required or not?

This is only conflict due to new revision of ISO 9001.  Since Manual is not required in 2015 updation, but it keeps value in companies.

So, what is a quality manual?

A quality manual describe the company’s intentions for operating the process of Quality Management System. It can include policies for all areas of the business its affect the ability to make high quality products which meets customers and ISO These policies define how your department managers will implement procedures within the boundaries specified in the quality manual.

An important note

Many other quality management system standards based on ISO 9001 are still requiring a quality manual. If your standard requires one, then you must maintain a quality manual.

Here are some uses for a quality manual.
  1. To communicate management’s expectations to employees
  2. To demonstrate the company’s plan to conform to the requirements of ISO 9001:2015
  3. To demonstrate the fulfillment of Clause 5.3, that organizational roles, responsibilities and authorities are assigned, communicated and understood
  4. To provide a starting point for auditors:
    1. Internal
    2. Customer
    3. ISO Certification Body
For users of ISO 9001:2015, the contents of your quality manual are completely up to you. But, remember that everything you say you do, you must show evidence that you really do it! So be careful what you include and make sure the policies reflect actual practices. Here are some common topics included in quality manuals:

  • Quality policy
  • Explanation of the company’s documentation structure
  • Organizational chart
  • Policy statements for each applicable ISO requirement
  • Reference to operating procedures
Of course, your quality manual may not cover each of these, and it may include much more. The trick is to find a balance between all that could be in there and what really needs “to be”.


To develop a quality manual, you might consider these steps:
  1. List policies to be written (note any ISO requirements that do not apply).
  2. Draft policies based on applicable ISO requirements.
  3. List operating procedures or refer to them as appropriate.
  4. Determine format and structure of the manual and make the first draft.
  5. Circulate the draft manual for input from all departments and address inadequacies identified.
  6. Attain a formal approval and release.
So many things are in Quality Manual. Its just a try to spread awareness for ISO 


Wednesday, 24 October 2018

What do you mean by "HACCP" ?

HACCP means hazard analysis critical control point. This tool is used to identify risk in food industry, when hazards have been identified then we have to take prevented action to stop it so quality of food products and concern party will not be effective.

There are several categories in Food Hazards including biological, chemical & physical depending on the types of food industry.

The 7 Principles of HACCP

There are 7 principles of HACCP which include conducting a hazard analysis, determining the Critical Control Points, establishing Critical Limits,  establishing corrective actions to apply when monitoring indicates a loss of control, the establishment of procedures for verification and the establishment of documentation and records.

1. Analysis of hazard

Identify the hazard in food industry ( production industry, manufacture industry and distribution industry). Assess the weak points  and measure for their control.

2. Determine the Critical Control Points

Determine the points, procedures or operational steps that can be controlled to eliminate the hazard(s) or minimize its (their) likelihood of occurrence.  A “step” means any stage in food production and/or manufacture including the receipt and/or production of raw materials, harvesting, transport, formulation, processing, storage, etc.

3. Identity Critical limit

Establish critical limit ensures the risk is under control. A critical limit is a criteria that separates acceptability from unacceptability. Critical limits may be descriptive or not.

4. Establish a system to monitor control of HACCP

Establish a system to monitor control of the HACCP by scheduled testing or observations. Monitoring is used to determine when a hazard maybe out of control. The frequency and method of monitoring needs to be established along with who is responsible for conducting the monitoring.

5. Corrective actions

Corrective action should be taken through industry because without corrective action how can we remove non conformity in our system. Through proper training staff will get to know which kind of corrective action they have to apply in industry.

6. Vehement procedures for verification

Verification should be very pure and and in a right direction. Auditor knows everything about standard he has quality to identify it . Auditor make sure that he never miss any non conformity in food industry because this is very necessary that company should maintain HACCP standard so quality of product can increase.

7. Maintain documentation and records

Proper record keeping is necessary for HACCP system. HACCP standard should be documented. Documentation and record Keeping should be maintain according to HACCP procedure.

In standard so many things are there but its just a try to aware regarding HACCP . So everyone knows that how standard is important for our life.