01 1BORAX FRANCAIS Coudekerque-Branche FR
01 1Borax, Granular and powder
01 1U.S.A
01 1Valid
Certificate Number : R1-CEP 2009-207 - Rev 05
Status : Valid
Issue Date : 2023-05-31
Type : Chemical
Substance Number : 13
22
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A Boric acid - Sodium tetraborate buffer solution manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boric acid - Sodium tetraborate buffer solution, including repackagers and relabelers. The FDA regulates Boric acid - Sodium tetraborate buffer solution manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boric acid - Sodium tetraborate buffer solution API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Boric acid - Sodium tetraborate buffer solution supplier is an individual or a company that provides Boric acid - Sodium tetraborate buffer solution active pharmaceutical ingredient (API) or Boric acid - Sodium tetraborate buffer solution finished formulations upon request. The Boric acid - Sodium tetraborate buffer solution suppliers may include Boric acid - Sodium tetraborate buffer solution API manufacturers, exporters, distributors and traders.
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A Boric acid - Sodium tetraborate buffer solution CEP of the European Pharmacopoeia monograph is often referred to as a Boric acid - Sodium tetraborate buffer solution Certificate of Suitability (COS). The purpose of a Boric acid - Sodium tetraborate buffer solution CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Boric acid - Sodium tetraborate buffer solution EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Boric acid - Sodium tetraborate buffer solution to their clients by showing that a Boric acid - Sodium tetraborate buffer solution CEP has been issued for it. The manufacturer submits a Boric acid - Sodium tetraborate buffer solution CEP (COS) as part of the market authorization procedure, and it takes on the role of a Boric acid - Sodium tetraborate buffer solution CEP holder for the record. Additionally, the data presented in the Boric acid - Sodium tetraborate buffer solution CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Boric acid - Sodium tetraborate buffer solution DMF.
A Boric acid - Sodium tetraborate buffer solution CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Boric acid - Sodium tetraborate buffer solution CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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