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WERCSmart Registration

UL WERCSmart Battery and Battery Products Registration ServiceUL WERCSmart is a platform that provides chemical compliance and supply chain management solutions for North American retailers, and has been promoted as a tool for reducing operational costs and risks in the US retail industry. Currently, nearly 9000 suppliers worldwide register their product information on this platform. The retailers that have cooperated with UL WERCSmart include 36 large retailers, including Wal Mart, Amazon, CVS, Lowe's, Meijer, Target, Staples, Walgreens, Sam's Club, O'Reilly, Costco, Korger, Sears, etc. Nowadays, WERCSmart evaluates over $1 trillion in global product trade annually, helping enterprises continuously meet global regulatory and compliance requirements.WERCS is a database company and a leading global supplier of green supply chain systems and chemical regulatory response software. Its software packages play an important role in helping customers manage product information and ...

2021 - 05 - 19
WEEE registration

WEEE refers to Waste Electrical and Electronic Equipment (WEEE) Directive (2002/96/EC)Scrapped electronic and electrical equipment has a detailed definition of 'waste' in Directive 75/442/EEC and has been modified in Directive 91/156/EEC. Scrapping actually refers to all categories of products in Annex I of the WEEE Directive, even if the product has not reached the end of its service life stage, as long as it is discarded by consumers, it is considered waste.Starting from August 13, 2005, manufacturers of electronic and electrical equipment circulating in the EU market must legally bear the responsibility of paying for the recycling of scrapped products. At the same time, EU member states are obligated to develop their own electronic and electrical product recycling plans and establish relevant supporting recycling facilities, so that end-users of electronic and electrical products can conveniently and freely dispose of scrapped equipment.Producer Responsibility:Design environ...

2017 - 09 - 19
FDA Food Registration

FDA Food RegistrationThe FDA's regulatory agency for food, agricultural products, and seafood is the Center for Food Safety and Nutrition (CFASAN), whose responsibility is to ensure that American food supply is safe, clean, fresh, and clearly labeled.Food certificationThe food supervised by the center imports $240 billion annually, of which $15 billion belongs to imported food. The main monitoring focuses of the center include:1. Freshness of food;2. Food additives;3. Food biotoxins and other harmful ingredients;4. Seafood safety analysis;5. Food labeling;6. Tracking and warning after food is launchedAccording to the anti-terrorism law passed by the United States Congress in 2003, food companies outside the United States must register with the FDA before exporting to the United States and provide shipping notifications to the FDA at the time of export. Foreign food production and processing companies that must register with the FDA under Public Law 107-188 of the United States are ...

2017 - 06 - 28
FDA Laser Registration

Laser certification1. Application FormApplication form: including company information, product information, etc2. Product File/Technology SpecificationProduct documents/technical materials: mainly including preparing detailed manuals/sales manuals, installation manuals, maintenance manuals, etc; Product assembly drawings; And product technical information, whether there are laser protection measures and a description of their working principles.3. LabelLabels: English labels that comply with regulations, including warning labels, product labels, compliance certification labels (such as Complaints with 21 CFR 1040.10&1040.11), and exit labeling labels, etc.4. Laser InformationLaser device information: Type of laser generator, medium, laser path diagram, laser parameters, laser device qualification certificate/test record (if purchased from other manufacturers, information of the manufacturer, laser device parameters/datasheet or manual, and whether the laser device has FDA certifica...

2017 - 06 - 28
FDA Medical Registration

The management of medical devices by the FDA is carried out through the Center for Devices and Radiological Health (CDRH), which supervises the production, packaging, and distributors of medical devices to comply with legal regulations in their business activities.The range of medical devices is very wide, ranging from medical gloves to cardiac pacemakers, all of which are under FDA supervision. Based on their medical use and potential harm to the human body, the FDA classifies medical devices into categories I, II, and III, with higher categories providing more supervision.If the product is a novel invention that has never existed in the market, the FDA requires manufacturers to conduct rigorous human experiments and have convincing medical and statistical evidence to demonstrate the effectiveness and safety of the product.The FDA certification of medical devices includes: manufacturer registration with FDA, product registration with FDA, product launch registration (510 form registra...

2017 - 06 - 28
Quebec Registration

TSSA is the abbreviation for Technical Standards&Safety Authority and is the Technical Standards and Safety Agency of Ontario, Canada. Responsible for safety certification services in areas such as pressure vessels, entertainment equipment, filler registration, and fuel.Quebec and Manitoba also have similar registration requirements. Therefore, if the product is exported to Canada without a clear sales province, Beide Testing recommends registering in each of the three provinces mentioned above to ensure smooth sales of the product in Canada.

2017 - 06 - 25

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