Major companies and all government-related organizations require that their suppliers comply with relevant industry standards.


Once you're certified you can expect:

More business opportunities
Dramatic reductions in operating costs
Greater profitability
Increased demand for your products and services
Better customer satisfaction
Improved working conditions

The House Of Quality experts can guide you through the standards certification requirements for your particular industry quickly, easily and painlessly.

As always, we are only a phone call or email away if you want to ask any questions or discuss how implementing these quality standards can benefit your business.

We know that implementing international quality standards may seem to be a daunting task at first. Click on the International Standards below for a brief description of each standard. We suggest you find out more details for your particular industry by following our links to more information.

ISO 9001:2000 - Quality Management Standard
ISO 13485 - Medical Devices Standard (additions to ISO 9001 standard)
ISO 14000 - Environmental Management Standard
TL 9000 - Telecommunication Providers Standard
CMM - Software Standard
GMP - Food and Drugs Administration (FDA) Rules (USA)
OHSAS 18001 - Occupational Health And Safety Management Systems Standard

 

ISO 9001:2000 - Quality Management Standard

When you're ISO 9001 certified, your partners in business know that quality objectives, continuous improvement, and customer satisfaction take centre stage in your company policy. ISO 9001 offers you a standard of excellence for everyday business processes. The House of Quality consultants take excellence a stage further and help you plan for  unexpected contingencies such as accidents or emergencies too.

ISO 13485 - Medical Devices Standard (additions to ISO 9001 Standard)

ISO 13485 deals with all medical devices and embraces the Good Manufacturing Processes (GMP) regulations in the USA. (The equivalent European standard is EN 46001 while the hardware and software are regulated by EN 46002.) The ISO 13485 standard is based on a process approach to quality management, where the supply chain concept is the same as ISO 9001. It stresses the relevancy of international and national regulations.

Back To Top

ISO 14000 - Environmental Management Standard

ISO 14000 is a global business initiative of the International Organization for Standardization. It aims at creating voluntary agreement worldwide on environmental management systems and provides tools for businesses to boost efficiency. ISO 14000 may become the global passport for environmentally responsible business, just as ISO 9000 set the standard for Quality Management. While ISO 14000 certification may mean clear environmental goals and regular performance reports, it is no guarantee of clean and efficient practices on the ground. The ISO standard is concerned with management systems rather than environmental pollution prevention or clean-up. After setting the environmental goals the next step is ensuring their implementation. Two draft documents are critical - ISO 14001 which is the core standard, and ISO 14004 which contains practical guidelines for implementation. The ISO 14001 standard is best when blended into ISO 9001 (manufacturing) and OHSAS 18001 (health and safety) in order to get a complete and consistent quality system.

Back To Top

TL 9000 - Telecommunication Providers Standard

The TL 9000 standard is developed and maintained by the Quality Excellence for Suppliers of Telecommunications (QuEST) Forum. It establishes a common set of quality system requirements, performance metrics, cost and quality indicators for suppliers of telecommunication products.

  TL 9000-HW - hardware
  TL 9000-SW - software
  TL 9000-SC -  services

The goals of TL 9000 are to

   foster quality systems that effectively and efficiently protect the integrity and use of telecom products and services
  drive continuous improvement
  enhance customer-supplier relationships

Our experts have participated in developing and validating cell phones software and hardware in Europe, South East Asia and Israel. We can help you achieve the European certification and be ready for TL 9000 audits.

Back To Top

CMM - Software Standard

The Capability Maturity Model Integration (CMMI) standard for software is divided into five Maturity Levels which indicate a set of process capabilities and contains Key Process Areas (KPA). These KPAs are devised to achieve goals and organized by Common Features, which are their attributes. They contain Key Practices (KP), which describe the activity to be performed or the infrastructure needed. The five Common Features are

the commitment to perform,
  the ability to perform,
  the activities performed (what is to be done, not how),
  measurements and analyses needed, and
  verifying the implementation (typically reviews and audits).

The Capability Maturity Model (CMM) standard is a relatively inexpensive standard to achieve since it allows self-assessment by each firm. It is also possible to apply for external certification. It is currently being expanded to include CMMP for tangible products. Our experts can help you implement the CMM methodology quickly and easily.

Back To Top

GMP - Food and Drugs Administration (FDA) Rules (USA)

The current Good Manufacturing Processes for the Food and Drugs Administration of the United States of America are a set of guidelines without which no drugs or food products can be commercialised in the USA. Moreover, the GMP standard is acknowledged the world over as generally the most stringent set of such rules. Whether you are an international pharmaceutical firm or a small catering company, adopting the GMP rules will help you provide the highest quality products to your clients.

OHSAS 18001 - Occupational Health And Safety Management Systems Standard

Originally an English standard, OHSAS 18001 has been adopted worldwide as a complementary standard to the ISO 9001 (manufacturing or service processes) and ISO 14001 (environment) standards. OHSAS 18001 is geared towards the continuous improvement of health and safety at work. Based on local legislation, it requires extra, voluntary steps towards reducing occupational illness and accidents at work. Together, the management and employees design an improved health and safety policy, plan an improvement process, train staff and implement the plan. There are periodic audits to confirm the plan's success. Our experts can help you design and implement OHSAS 18001 in your company.

Back To Top


Home     About Us      Our Services     International Standards     Our Clients       
Links
      Contact Us       עברית