SPI Pharma has been solving formulation challenges using superior functional materials.
01 2SPI PHARMA, INC. Wilmington US
02 1ALUPHARM Compiègne FR
03 1BRENNTAG BIOSECTOR A.S. Frederikssund DK
04 1Ferro Corporation Independence US
05 1Ferro Corporation Walton Hills US
SPI Pharma has been solving formulation challenges using superior functional materials.
Aluminium Oxide, Hydrated, 0325
Certificate Number : CEP 2008-270 - Rev 01
Status : Valid
Issue Date : 2025-03-25
Type : Chemical
Substance Number : 311
SPI Pharma has been solving formulation challenges using superior functional materials.
Aluminium Oxide, Hydrated, 0200
Certificate Number : CEP 2008-264 - Rev 01
Status : Valid
Issue Date : 2025-03-26
Type : Chemical
Substance Number : 311
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A ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1), including repackagers and relabelers. The FDA regulates ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) 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 ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) supplier is an individual or a company that provides ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) active pharmaceutical ingredient (API) or ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) finished formulations upon request. The ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) suppliers may include ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) API manufacturers, exporters, distributors and traders.
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A ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP of the European Pharmacopoeia monograph is often referred to as a ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) Certificate of Suitability (COS). The purpose of a ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) to their clients by showing that a ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP has been issued for it. The manufacturer submits a ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP (COS) as part of the market authorization procedure, and it takes on the role of a ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP holder for the record. Additionally, the data presented in the ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) DMF.
A ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1) 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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We have 5 companies offering ALUMINUM (SEE ALSO ALUMINUM OXIDE 1344-28-1)
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