Total Quality Management Consultants is a Consultancy Agency eatablished in Mumbai, India to assist you for ISO 9001, ISO 14001, ISO 27001 (BS 7799), ISO/TS 16949, OHSAS 18001, ISO 22000 (HACCP), cGMP certification, and UL, CE, CSA Marking (certification)
Now after establising its credentials in India, TQMC has now set up representatives in the Gulf region, Malaysia and California, USA.
The CEO, S.X. D'Souza is a Mechanical Engineering graduate of I.I.T Kanpur with an experience of 21 years in Quality Control in Engineering Industry. He established his credentials by appearing for the CQA - ASQC (Certified Quality Auditor - American Society for Quality Control, and now referred to as ASQ) exam in 1994, and was the only candidate in India to have passed the exam, then.
Babu Mendes is now a partner in TQMC operations.
Today, Total Quality Management Consultantsis recognized by all the major certification bodies in India.
Click here to have a look at the sectors we have covered so far.
To uphold and advance the honor and dignity of the profession, and in keeping with high standards of ethical conduct, Total Quality Management Consultants subscribe to the ASQcode of ethics
Aside from Management Systems TQMC has also established hard core competencies in :
• Business risk assessment and Business Turnaround • Technology upgradation • Process control instrumentation • ERP • Six Sigma (free)
ISO 9001 revision expected to be released in August 2008, read more
Union Govt. toughens norms for selection of consultants for ISO 9001/ ISO 14001 certification. Go here
ISO 22000 and FOOD SAFETY The Food and Agriculture Organisation (FAO) and the World Health Organisation (WHO) established the Codex Alimentarius Commission in 1962 relating to Food safety, this formalised the world-wide approach to ensure safe food. HACCP (Hazard Analysis and Critical Control Points) a method to prevent unsafe food, plays an important role. Today in the European Union (EU), the United States, Canada and other countries the implementation of HACCP is mandatory.
ISO 22000 is all encompassing and includes all branches of the food chain including equipment suppliers, services for cleaning of equipment and also animal and plant feed mixtures and additives.
Benefits of HACCP System
Giving the confidence that the food products have been produced safely and hygienically. HACCP demonstrates due diligence in the hygienic production of the products.Implementation of HACCP System is required by law in most countries of the world. It is also a cost-effective way to reduce wastage and recalls.
ISO 22000 go here Total Quality Management Consultants is reputed to be one of the best Food Safety consultants in India catering to all food service providers in the food supply chain. more…
What Is GMP?
GMP refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act (See Chapter IV for food, and Chapter V, Subchapters A, B, C, D, and E for drugs and devices.) These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous. Failure of firms to comply with GMP regulations can result in very serious consequences including recall, seizure, fines, and jail time.
when all of the oceans and lakes are polluted when the greenhouse effect takes its toll and temperatures rise and melt the poles
when the blue birds stop singing and trees stop flowering
and the moon decides not to rise and mother nature up and dies
and caterpillars turn to stone and the world finds itself alone
and all the fuel is finally depleted and all the farmers chores are completed and the Earth stands still, devoid of weather..
then it is too late, my friend
- forwarded by Kathy in USA, author unknown
Environmental credibility is becoming a factor in national and international competitiveness.Created by the International Organization for standardization (ISO), ISO 14001 is based on the two concepts of continual improvement and regulatory compliance. The standard contains the core elements for an effective EMS and can be applied to any type of organisation in any sector.
Benefits of ISO 14000
Environmental management affects your bottom line by improving your processes through:
· Cutting costs, e.g. energy, waste, raw materials
· Ensuring compliance with regulatory and legal requirements
· Building public image towards clients, regulatory bodies and other stakeholders
· Motivating your employees
Total Quality Management Consultants provide the best consultants in India for implementing ISO 14001 EMS more....
OHSAS 18001
Companies today are expected to demonstrate a sincere commitment to the health, safety and well being of their employees. Knowledge of your workplace hazards and ways to eliminate them can improve the management and operations of your company while lowering expenses and improving employee morale.
Organizations in many sectors have realized the internal and external benefits of implementing a sound health and safety management system giving them the structure and control necessary to monitor management practices that result in reduced costs and risks associated with their manufacturing processes.
An independent assessment of your Occupational Heath and Safety System is not only an excellent means of ensuring your safety system is working and protecting your staff, but it also sends a clear message to stakeholders and authorities that you have adopted good safety practices.
In addition, an effective Health and Safety management system demonstrates a risk management approach that will help to reduce accidents and ill health leading to reduced downtime and related expenses. Many have implemented health and safety management systems as a means to help them achieve their corporate objectives while improving the bottom line. Regulatory compliance is a prime objective of an efficient Health and Safety program, but more importantly it provides an organized system ensuring that employees' health needs and concerns are addressed.
There are several excellent consensus standards and guidance documents available for example, OHSAS 18001
Total Quality Management Consultants has the best consultants in India for developing your ISO 18001 integrated with ISO 9001 QMS
SA 8000
The SA 8000 standard stipulates the following nine requirements:
·Minimum age:
Child labour, defined by the ILO as work carried out by children aged 15 years and younger (14 years in some exempted areas) is not permitted. Where practiced, child labour must be progressively eliminated in a constructive way so as not to make the child's economic situation worse.
· Forced labour:
Prohibited. Workers cannot be required to surrender identity papers, or pay "deposits" in order to gain employment.
· Occupational health and safety:
Companies must meet basic standards for a safe and healthy working environment. · Freedom of association and the right to organise : Protects the rights of workers to form and join trade unions or other organised groups where unions are prohibited by law.
· . Discrimination :
Prohibits discrimination on the basis of race, caste, nationality, religion, disability, gender, sexual orientation, union membership or political affiliation.
· Disciplinary practices:
prohibits corporal punishment, mental or physical coercion and verbal abuse of workers.
· Hours of work :
A regular working week is defined as that set out by local 1aw or 48 hours, whichever is shorter. Overtime is not to exceed 12 hours per week, even when the regular working week is less than 48 hours.
· Wages:
Must meet all minimum legal standards and provide sufficient income for basic needs.
· Management systems :
Define procedures for the effective management, implementation and auditing of SA8000 compliance
For more details, refer to the standard.
Total Quality Management Consultants has the best consultants in India for developing your SA 8000 Sysiem integrated with ISO 9001 QMS
As an alternative to BS 7799, ISO has now made available ISO 17799 and ISO 27001 read more
ISO 27001 and INFORMATION SECURITY MANAGEMENT
Code of practice, Controls needed:
Security Policy
Security organization
Asset classification and control
Personnel security
Physical and environmental security
Communications and operations management
Acccess control
Systems development and maintenance
Business continuity management
Compliance
Steps required for certification:
Developing Information Security policy
Scope statement
Doing risk analysis
Statement of applicability
Business Continuity plan
Designing the Management System
Implementation
Certification audit
ISO/IEC 27001 is the international version of the long standing BS7799-2. From October 2005, ISO 27001 has replaced BS7799-2:2002 as the international information security management systems standard. From now on, ISO 27001 is the standard against which an ISMS will need to be certified, and it's the standard that increasingly organizations will use to demonstrate regulatory compliance and effective business risk management.
FLASH NEWS !
ISO/IEC 17025:2005, General requirements for the competence of testing and calibration laboratories, replaces the 1999 edition which has been used to "accredit" (approve) some 25 000 laboratories worldwide that test products and samples, and calibrate precision instruments. However, the influence of ISO/IEC 17025 is even greater than this figure suggests since many countries make its use a legal requirement. In addition, documents derived from it are used by laboratories in specific sectors such as medicine and microbiology. ISO Secretary-General Alan Bryden commented: "ISO/IEC 17025 benefits business, government and society at large. Confidence in the competence of laboratories is frequently needed by businesses when testing new products, or ensuring that finished products are fit for sale, by government regulators and trade officials that require assurance about domestic or imported products before they can be placed on the market, or for ensuring the quality and reliability of testing and analysis relating to environmental, health or safety hazards."
ISO/IEC 17025:2005 contains all of the requirements that testing and calibration laboratories need to meet in order to demonstrate to customers and regulators that they operate a sound management system which puts them in full control of their processes, are technically competent, and are able to generate technically valid results. Accreditation bodies that recognize the competence of testing and calibration laboratories will use the standard as the basis for their accreditation.
"Dependable testing and calibration laboratories are ones that have been duly accredited as competent and ISO/IEC 17025:2005 is the laboratory accreditation standard that, like the edition it replaces, will be counted on by business and governments worldwide," declared Peter van Leemput, who led the ISO group of experts that carried out the work.
The new, 2005 edition results from the amendment of ISO/IEC 17025:1999 to ensure its compatibility with the requirements of ISO 9001:2000, Quality management systems - Requirements. This became necessary because of the generalized adoption of quality management systems conforming to ISO 9001:2000, including many of the organizations that testing and calibration laboratories serve.
It also seeks to clarify that while compatible, the two standards are not inter-changeable. Although both standards can be used by laboratories as a framework for providing their customers with confidence that they are managing their activities, only ISO/IEC 17025 can be used to demonstrate the technical competence specific to laboratories.
Laboratories may choose to be accredited to ISO/IEC 17025, or be certified to ISO 9001:2000, or both, but the processes of accreditation and certification would still be two separate actions, although highly facilitated - both for the laboratories and the assessors - by the consistency now ensured between the two standards.
There are no essential changes to the technical requirements. The modifications relate mainly to the management requirements in the document to reflect the content of ISO 9001:2000, especially in a greater emphasis on the responsibilities of top management, on the need to demonstrate a commitment to continually improve the effectiveness of the management system, on customer satisfaction, and on internal and customer communication about the management system.
Peter van Leemput summed up: "Laboratories that have described and controlled their processes within the laboratory - as already required by the 1999 edition of ISO/IEC 17025 - will only have minor adjustments to make to their existing procedures to ensure that the new orientations in the management requirements are fulfilled."
The International Laboratory Accreditation Cooperation (ILAC) has set a transition period of two years from date of publication of the new edition - 12 May 2005 - for accredited laboratories to comply with the standard's requirements. In India the body that certifies labs is NABL, go here http://www.nabl-india.org/nabl/html/faq.asp
National Accreditation Board for Testing and Calibration of Laboratories (NABL) has come up with a new standard, ISO: 15189: 200, for evaluation of quality of work and competency of medical laboratories. This new standard will become effective in India from June 1, 2005.
As of now, about 40 medical laboratories across the country have been accredidated by NABL under earlier standard ISO: 17025:1999. These laboratories will have to upgrade to ISO:15189:2003 by June 30, 2005.
Principles of CE marking The CE marking symbolises the conformity of the product with the applicable Community requirements imposed on the manufacturer.
The CE marking affixed to products is a declaration by the person responsible that: * the product conforms to all applicable Community provisions, and * the appropriate conformity assessment procedures have been completed. to substantially modified products that are subject to directives as new products.
Directives may exclude the application of the CE marking on certain products, even if the directive otherwise applies to the product. As a general rule, such products are subject to free circulation (125), if: they are accompanied by a declaration of conformity (as is the case for safety components referred to in the Directive on machinery and partly completed boats referred to in the Directive on recreational craft); they are accompanied by a declaration of compliance (as is the case for products playing a minor part with respect to the health and safety listed in accordance with the Directive on construction products); they are accompanied by a statement (as is the case for custom-made medical devices and devices intended for clinical investigations referred to in the Directives on active implantable medical devices and medical devices, and devices intended for performance evaluation referred to in the Directive on in vitro diagnostic medical devices);
Products to be CE marked The CE marking is mandatory and must be affixed before any product subject to it is placed on the market and put into service, save where specific directives require otherwise.
Where products are subject to several directives, which all provide for the affixing of the CE marking, the marking indicates that the products are presumed to conform to the provisions of all these directives.
A product may not be CE marked, unless it is covered by a directive providing for its affixing. The obligation to affix the CE marking extends to all products within the scope of directives providing for its affixing, and which are intended for the Community market (124).
Thus, the CE marking must be affixed: to all new products, whether manufactured in the Member States or in third countries; to used and second-hand products imported from third countries; and
Affixing of the CE marking The CE marking must be affixed by the manufacturer, or by the authorised representative established within the Community. The CE marking must take the form below. If the CE marking is reduced or enlarged the proportions must be respected.
The CE marking must be affixed visibly, legibly and indelibly to the product or to its data plate. However, where this is not possible or not warranted on account of the nature of the product, it must be affixed to the packaging, if any, and to the accompanying documents, where the directive concerned provides for such documents.
Where a notified body is involved in the production control phase according to the applicable directives, its identification number must follow the CE marking. The manufacturer or the authorised representative established in the Community affixes the identification number, under the responsibility of the notified body
TQMC has assisted and guided many clents in obtaining CE Marking. TQMC does not charge for this service. Only if you require a management system (speciied by the EU Directive for High Risk products) we will charge. Or if u want us to develop your TCF. the service is chargeable.
Refer to the CE Marking link below for more information on line.
GS Mark
The GS Mark is a German safety mark, indicating that a
product has been tested and found to comply with the safety
requirements of European Standards with the German national
deviations. GS stands for geprüfte Sicherheit or “safety
tested”.
The GS Mark is a voluntary mark that is highly regarded
by both consumers and manufacturers in the German
speaking countries of Central Europe –
Germany, Austria
and Switzerland
– with a population of approximately 100
million people. It can be found on electrical, mechanical or
electromechanical equipment and it proves that a product
has been verified by an accredited third party, in other
AS 9100:2001 Aerospace Standard When the aerospace industry realized that it was necessary to supplement the ISO quality management system model to satisfy internal, government and regulatory requirements for the aerospace industry, AS 9100 was established. This standard comprises the ISO 9001:2000 requirements augmented by aerospace industry requirements. It was the result of an international effort by aerospace companies with a common goal of establishing a quality management system for use within the aerospace industry.
To assure customer satisfaction, aerospace industry organizations must produce, and continually improve safe, reliable products that meet or exceed customer and regulatory requirements. The globalization of the aerospace industry, and the resulting diversity of regional/national requirements and expectations, has complicated this objective. End-product organizations face the challenge of assuring the quality of, and integration with, product purchased from suppliers throughout the world and at all levels within the supply chain. Aerospace suppliers and processors face the challenge of delivering product to multiple customers having varying quality expectations and requirements.
TL 9000 TL 9000 requirements were developed by the QuEST forum (The Quality Excellence for Suppliers of Telecommunications Leadership), comprised of leaders in the telecommunications field. The QuEST forum used ISO 9000 as a baseline and the requirements of existing industry standards and practices in developing the TL 9000 requirements. The development of sector-specific requirements for hardware, software and services quality system and metrics requirements is an essential part of TL 9000. For more information or to order a copy of the Standard, please go to the QuEST Forum Web site www.questforum.org or the American Society for Quality at www.asq.org.
Total Quality Management Consultants will soon be certified to ISO 9001 as a service provider.
Scope: Providing consultancy in the field of Management Systems and CE Marking and as a Human Resource Development Centre by providing Training to Organizations. Location: Mumbai, India.