European certifications are:
1, European EN71 certification (toys);
EN71 is the European Union market specification for toy products. Children are society's most concerned about and love the group, children generally love the rapid development of the toy market, while all kinds of toys due to various quality problems to children's injuries also occur from time to time, so the world's countries on the market for their own toys are becoming increasingly stringent requirements.
Many countries have established their own safety regulations for these products, and manufacturing companies must ensure that their products meet the relevant standards before they are sold in the region. Manufacturers must be held responsible for accidents caused by production defects, poor design or the use of inappropriate materials. This led to the introduction of the EN71 certification decree for toys in Europe, the significance of which is the technical regulation of toy products entering the European market by means of the EN71 standard, so as to minimize or avoid the harm of toys to children.
2, the European Union EMC electromagnetic compatibility certification;
EMC (Electromagnetic Compatibility) full name is Electro Magnetic Compatibility, which is defined as "equipment and systems in its electromagnetic environment can work properly and does not constitute an intolerable electromagnetic harassment of anything in the environment," the definition contains two meanings. "The definition contains two meanings, first, the equipment should be able to work in a certain electromagnetic environment, that is, the equipment should have a certain degree of electromagnetic immunity (EMS); Second, the equipment itself produces electromagnetic harassment can not produce excessive impact on other electronic products, that is, electromagnetic harassment (EMI).
3, the European Union MDD certification;
MDD is the European Union Medical Devices Directive 93/42/EEC abbreviation for medical devices sold in the European Union countries for certification, is mandatory certification, the need to be authorized by the announcement of the agency to certify, such as the TUV, Switzerland, SGS and so on.
MDD is an acronym for Medical Device Directive. The European Union CE marking below a directive for medical devices. MDD directive products are divided into three classes: Class I, Class II, Class III, the higher the hazard level of the product classification of the higher level, the more stringent the certification, the longer the cycle, the higher the cost.
4, the European Union GMP certification;
GMP is an acronym for GOOD MANUFACTURING PRACTICE, the Chinese meaning is "Good Manufacturing Practice". The World Health Organization defines GMP as a regulation that guides the production and quality management of food, drugs and medical products.
GMP is a set of mandatory standards for the pharmaceutical, food and other industries, requiring companies to meet hygiene and quality requirements from raw materials, personnel, facilities and equipment, production processes, packaging and transportation, quality control and other aspects of the relevant national regulations to form a set of operational practices to help companies to improve the health of the corporate environment, and to identify problems in the production process in a timely manner, to improve.
Briefly, GMP requires pharmaceutical, food and other production enterprises should have good production equipment, reasonable production process, perfect quality management and strict testing system to ensure that the final product quality (including food safety and hygiene) in line with regulatory requirements.
5, the European Union CE safety certification;
CE certification, that is, limited to the product does not jeopardize the safety of human beings, animals and goods in terms of basic safety requirements, rather than the general quality requirements, the harmonization of the directive only provides for the main requirements of the general directive requirements is the task of the standard. Therefore, the precise meaning is: CE mark is a safety mark rather than quality mark. It is the "main requirements" that form the core of the European Directive.
The "CE" mark is a safety certification mark, considered as a passport for manufacturers to open and enter the European market. CE stands for European harmonization (CONFORMITE EUROPEENNE).