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Inspection
1. Introduction of inspection serviceWhether you are a trader, e-commerce platform, brand owner or manufacturer, whether you are concerned about supplier selection or raw material procurement, production, packaging and transportation, Lanya can formulate a complete personalized quality control plan for you. Reduce sourcing risk for you and ensure that any product in your supply chain meets quality and safety standards.2. Service Category1. Factory review2. Pre-production inspection3. Mid-production inspection4. Random sampling inspection at the end of production5. Inspection before shipment6. Loading inspection3. Common productsElectrical and electronic products, accessories for electronic products, IT products, lighting products, batteries, toys and handicrafts, ceramics and other handicrafts, miscellaneous goods 4. Auditing Service Auditing Service1. Introduction of Lanya Audit ServiceInspect your facilities, equipment and products and audit your systems and processes against any local or global reference standard. In many cases, we will issue certification to your organization based on the results of inspections and audits.contact usLanya Technology Service (Shenzhen) Co., Ltd. is an accredited laboratory by international institutions such as National CNAS, China Metrology Certification CMA, American Laboratory Accreditation Association A2LA, Wireless Power Consortium WPC, Bluetooth Certification and Evaluation Committee SIG Amazon Amazon, etc. Lanya's mission: to make...
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ISO13485 Medical Device Management System
ISO13485 is called "medical device quality management system" in Chinese. Since medical devices are special products that save lives, heal the wounded, prevent and cure diseases, it is not enough to standardize only the general requirements of the ISO9000 standard. /T0287 and YY/T0288), put forward special requirements for the quality management system of medical device manufacturers, which has played a good role in promoting the quality of medical devices to be safe and effective.IntroductionThe full name of the ISO13485:2003 standard is "Medical device-Quality management system-requirements for regulatory". The standard is formulated by the SCA/TC221 Medical Device Quality Management and General Requirements Standardization Technical Committee and is an independent standard based on ISO9001:2000. The standard specifies the quality management system requirements for relevant organizations, but it is not a guide for the implementation of the ISO9001 standard in the medical device industry.Since the standard was released in 1996, it has been widely implemented and applied all over the world. The new ISO13485 standard was officially released on July 3, 2003. Different from the ISO9001:2000 standard, ISO13485:2003 is a management standard applicable to a regulatory environment: from the name, it is clearly a quality management system requirement for regulations. Internationally, medical devices are not only general marketed commodities operating in a commerci...
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OHSAS18001 Occupational Health and Safety Management System
1. Introduction to CertificationOccupational health and safety management system (OHSAS) is a modern safety production management model that emerged internationally in the late 1980s. It is called a post-industrial epoch-making management method together with the management systems stipulated by ISO-9001 and ISO14001 standards. The OHSAS18001 standard is currently the only standard that can be used for third-party certification. This standard provides a structured operating mechanism for various organizations to help organizations improve safety production management, promote occupational health and safety and continuous improvement. After the OHSAS18000 standard was promulgated, it immediately aroused great repercussions around the world. Many countries and certification bodies took it as the standard for implementing certification. According to the current international demand and implementation of the standard, the standard has become widely used. The most authoritative occupational health and safety management system standard.OHSAS18000 standard certification helps to promote the organization itself to meet the requirements of relevant laws and regulations; reduce failure costs; improve production efficiency; promote the development of economic and trade activities; establish a good corporate image.contact us:Lanya Technology Service (Shenzhen) Co., Ltd. is an accredited laboratory by international institutions such as National CNAS, China Metrology Certification CMA, Ame...
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ISO14001 Environmental Quality Management System
1. Introduction to CertificationThe ISO14001 standard is produced under the background of serious environmental problems (such as greenhouse effect, ozone layer destruction, biodiversity destruction, ecological environment deterioration, marine pollution, etc.) facing human society today. It is the crystallization of the experience of environmental management in industrialized countries. The basic idea is to guide the organization to establish a self-restraint mechanism for environmental management in accordance with the PDCA model. From the top leader to each employee, they should actively and consciously handle the relationship between their own development and environmental protection, and continuously improve environmental performance. Pollution prevention, and ultimately achieve the benign development of the organization. The standard is applicable to organizations of any type and size, and to a variety of geographic, cultural and social environments.The International Organization for Standardization (ISO) officially promulgated ISO14001:1996 "Environmental Management System - Specifications and Guidelines for Use" in 1996. In order to clarify and clarify the requirements of the ISO14001 standard, ISO revised the standard, and in November 2004 On May 15, the new version of the standard ISO14-001:2004 environmental management system requirements and usage guidelines were promulgated. This standard is the core of the ISO14000 series of standards. It requires the ...
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COC human rights audit
Human rights factory audits are officially called social responsibility audits, social responsibility audits, social responsibility factory assessments, etc. It is further divided into corporate social responsibility standard certification and customer-side standard audit. This "factory audit" is mainly implemented in two ways.1 Corporate Social Responsibility Standard CertificationCorporate social responsibility standard certification refers to the activity in which the corporate social responsibility system developer authorizes some neutral third-party organizations to review whether the enterprises that apply for passing a certain standard can meet the specified standards. It is the purchaser that requires Chinese enterprises to pass certain international, regional or industry "social responsibility" standard certification and obtain qualification certificates as a basis for purchasing or placing orders. Such standards mainly include SA8000, ICTI (toy industry), EICC (electronic industry), WRAP (clothing, footwear and hat industry) in the United States, BSCI (all industries) in continental Europe, ICS (retail industry) in France, and ETI in the United Kingdom. (all industries) etc. [1]2Customer-side standard auditCustomer-side standard audit (Code of Conduct) is a multinational company, before purchasing products or placing production orders, to Chinese enterprises in accordance with the social responsibility standards formulated by multinational compan...
