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    An NDC code is an 11-digit identifier assigned by the FDA to identify a drug and its packaging. The NDC stands for National DrugCode, the "National DrugCode," which was introduced by the FDA in 1969. The NDC code consists of three parts, which are the drug manufacturer, the description of the drug and the package, and the package specification and quan
    May. 15th, 2021
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    Chemical and enterprise identification, composition/composition information, hazard overview, first aid measures, fire protection measures, leakage emergency treatment, handling and storage, contact control/personal protection, physical and chemical properties, stability and reactivity, toxicology data, ecological data, waste disposal, transportation i
    Dec. 15th, 2020
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    "Dangerous Goods Information" column has 5 sub-items, according to the condition of the goods truthfully fill in. Note: Whether the goods are dangerous goods is based on the Model Recommendation Regulations on the Transport of Dangerous Goods.
    Oct. 12th, 2020
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    Principle: "Classify first, then return to danger", on the basis of accurate classification, and then choose the most appropriate "inspection and quarantine name". The "inspection and quarantine name" of hazardous chemicals is generally "HS name + parenthetical note", and the naming structure of the note is "hazardous chemicals + main transportation r
    Sep. 05th, 2020
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    "One book, one signature" refers to the safety technical specifications and safety labels of chemicals. Chemical Safety Technical Specifications (SDS), also known as Material safety Technical specifications (MSDS) in some countries. SDS provides information on chemical safety, health and environmental protection, recommends protective measures and emer
    Aug. 15th, 2020
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    The time for FDA NDC registration varies depending on the completeness of the materials provided by the applicant and typically takes several months to a year for approval.
    Jul. 25th, 2020
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    MSDS is a comprehensive regulatory document on chemical characteristics provided by chemical production, trade and sales enterprises to downstream customers and the public according to legal requirements. Basic requirements for MSDS writing: 1, the format must be standardized, and the content of SDS must be arranged in strict accordance with the prepa
    Jul. 25th, 2020
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    1. The enterprise is ready to submit the product information to the testing institution, and the testing institution will evaluate the sample and quote the price 2. Both parties sign the contract 3. Testing institutions arrange testing 4. After the test is completed, the testing agency will issue a draft certificate and a draft report to the enterpr
    Jul. 15th, 2020
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    TSCA applies to naturally occurring and chemically reactive chemicals themselves, chemicals in mixtures, and intentionally released chemicals in articles. It is important to note that chemicals defined by TSCA also include microorganisms. If your products are pesticides (excluding pesticide intermediates), nuclear materials, food, food additives, pharm
    Jun. 21th, 2020
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    MSDS/SDS does not have a definite expiration date. But MSDS/SDS are not set in stone. The MSDS/SDS should be updated in time if: 1. When the regulatory basis and requirements formulated by SDS/MSDS are changed; 2. When the substance/ratio/composition of the product targeted by SDS/MSDS changes; 3. When the products targeted by SDS/MSDS are found to
    Jun. 15th, 2020
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