iso certification pakistan

Total Quality Management (TQM) is a systematic approach designed to help businesses progress their practices to more predictably lead to a constantly high quality product. Training in TQM is more commonly available at certificate and graduate certificate levels, but master’s degree programs also offer training in this business philosophy. The total in TQM applies to the complete organization. Therefore, unlike an ISO 9000 initiative which may be limited to the procedures producing deliverable products, TQM applies to each activity in the organization. Also, unlike ISO 9000, TQM covers the soft issues such as ethics, attitude and culture. The Total Quality Management Certification Test checks your information about the significant concepts, skills and techniques associated to the art of Total Quality Management. This test covers all the aspects of the art of Total Quality Management like meaning, concepts, foundation and principles of Total Quality Management, the quality managemen

A GMP is a system for making sure that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. GMP is an abbreviation for Good Manufacturing Practices. GMP is an initiative of the WHO. The main aim of GMP is to see to it that the products are good sufficient for utilization after the final outcome. GMP governs the product at each and every step of manufacturing. Good Manufacturing Practice (GMP) is that part of quality assurance which ensures that medicinal products are consistently produced and controlled to the quality standards appropriate to their intended use and as essential by the marketing authorization (MA) or product specification. GMP is concerned with both production and quality control. A Good Manufacturing Practices (GMP) certification scheme provides independent verification and certification that the

BIFMA’s sustainability certification program for furniture which includes performance necessities that address economic, environmental, and social responsibility throughout the supply chain. BIFMA e3 is applicable to manufacturers of business and institutional furniture and looks for to provide measurable market-based definitions of increasingly more sustainable furniture. BIFMA e3 certification is necessary by many organizations including the U.S. Government, who now needs e3 Gold standard certification from all suppliers of office furniture. The e3 standard (Economy, Energy and the Environment) was initiated by the U.S. government to encourage more environmentally sustainable practices in the manufacturing sector. Certification also applies toward points in the EPA Leed Certificate program. Furniture in office environments can take a lot of mistreatment. That’s why furniture manufacturers voluntarily conduct third-party testing for presentation and durability characteristics, to m

Basically put, GREENGUARD Certification makes sure that a product has met some of the world’s most rigorous and comprehensive standards for low down emissions of volatile organic compounds (VOCs) into indoor air. The GREENGUARD Certification Program (formerly known as GREENGUARD Indoor Air Quality Certification) gives assurance that products designed for use in indoor spaces meet strict chemical emissions limits, which contribute to the creation of healthier interiors. Achieving GREENGUARD Certification gives credibility to manufacturers’ sustainability claims, backing them with empirical technical data from an unbiased, third-party organization. If a product has been GREENGUARD Certified, it has been tested and systematically proven to have low chemical emissions, says Scott Steady, product manager for indoor air quality at UL Environment. In other words, it’s guaranteed to provide off only low levels of volatile organic compounds, or VOCs. GREENGUARD Certification standards ha

Muslims commonly use two terms to explain every subject as Halal or Haraam. Halal is a Arabic word which means allowable, lawful with respect to which no restriction exists, and the doing and consuming of which the Law-giver, Allah has permitted. Halal means the opposite-unlawful that which the Lawgiver completely prohibited; anyone who engages in it is liable to incur the penalty of Allah in the Hereafter as well as a legal punishment in this world. Halal is universal terms that affect to all facets of life. However, we use these terms only in relation to meat products, food ingredients, cosmetics, food products, personal care products, and food contact materials. There are some things which are not clear are considered questionable or suspect and more information is required to categorize them as Halal or Haram. If a muslim consumes Haram foods and materials, he would be sinful. Halal in terms of food means that food must be: Does not stem from or consists any part or item f

What is GOST R Certification? The GOST R certification system concerns the majority of products sold or/and used in Russia, namely: consumer products such as foodstuff, textiles, cosmetics and toys, mechanical and electrical goods, industrial equipment for food, chemical, oil & gas, construction and other industries. Is Russian Certification required for my products? Russia is an unique country and has unique requirements of safety. If you plan to trade with Russia, you should know and understand the Russian requirements for certification. Your products have to meet Russian standards which are different and mostly not harmonized with the European or International standards. CE self-declaration is not sufficient in Russia and cannot replace the Russian Certificate of Conformity. Basically, almost all consumer products require the mandatory certification. It includes all building materials, shoes, furniture, tableware and kitchenware, packaging materials, household and indu

What does CE marking mean? What do the initials CE stand for? CE marking is a declaration by the manufacturer that the product meets all the appropriate provisions of the relevant legislation implementing certain “European Directives”. “CE marking” gives companies easier access into the European market to sell their products without adaptation or rechecking. The initials “CE” do not stand for any specific words but are a declaration by the manufacturer that his product meets the requirements of the applicable European Directives. Does my product require the CE marking? You need to establish first which, if any, of the New Approach Directives or older Global Approach Directives applies to your product. CE marking only applies to products within the scope of these Directives. It should not be applied to products if they are outside the scope of the Directives. The European Commission’s lists Directives where the CE Marking will be applicable. It is available for purchase from the

ISO standards are reviewed every five years and revised if required. This supports make sure they remain helpful tools for the market. The challenges faced by business and organizations today are very different from a few decades ago and ISO 9001 has been updated to take this new environment into account. Both old and new standards cover effectively the same topics. However, there are some essential differences. Some of these are discussed below. Structure of the standard A general structure is possible because basic concepts such as management, client, needs, policy, procedure, planning, performance, objective, control, monitoring, measurement, auditing, decision making, corrective action, and nonconformity are general to all management system standards. While this will make it easier for organizations to implement multiple standards because they will all share the same basic needs, it may cause some disturbance in the short run as organizations get used to the new structure.