01 1PIERRE FABRE MEDICAMENT Gaillac FR
02 1Pierre Fabre Medicament Gaillac FR
03 1Pierre Fabre Santé - Plantes & Industrie Gaillac FR
01 1MicroCrystalline Hydroxyapatite Compound
02 2Ossein Hydroxyapatite Compound
01 3France
01 2Valid
02 1Withdrawn by Holder
Ossein Hydroxyapatite Compound
Certificate Number : R1-CEP 2001-133 - Rev 01
Status : Valid
Issue Date : 2014-01-10
Type : TSE
Substance Number :
Ossein Hydroxyapatite Compound
Certificate Number : R1-CEP 2006-047 - Rev 03
Status : Valid
Issue Date : 2021-01-22
Type : TSE
Substance Number :
MicroCrystalline Hydroxyapatite Compound
Certificate Number : R0-CEP 2001-132 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2001-12-20
Type : TSE
Substance Number :
A HYDROXYPROPYLMETHYLCELLULOSE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HYDROXYPROPYLMETHYLCELLULOSE, including repackagers and relabelers. The FDA regulates HYDROXYPROPYLMETHYLCELLULOSE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HYDROXYPROPYLMETHYLCELLULOSE 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 HYDROXYPROPYLMETHYLCELLULOSE supplier is an individual or a company that provides HYDROXYPROPYLMETHYLCELLULOSE active pharmaceutical ingredient (API) or HYDROXYPROPYLMETHYLCELLULOSE finished formulations upon request. The HYDROXYPROPYLMETHYLCELLULOSE suppliers may include HYDROXYPROPYLMETHYLCELLULOSE API manufacturers, exporters, distributors and traders.
click here to find a list of HYDROXYPROPYLMETHYLCELLULOSE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A HYDROXYPROPYLMETHYLCELLULOSE CEP of the European Pharmacopoeia monograph is often referred to as a HYDROXYPROPYLMETHYLCELLULOSE Certificate of Suitability (COS). The purpose of a HYDROXYPROPYLMETHYLCELLULOSE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of HYDROXYPROPYLMETHYLCELLULOSE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of HYDROXYPROPYLMETHYLCELLULOSE to their clients by showing that a HYDROXYPROPYLMETHYLCELLULOSE CEP has been issued for it. The manufacturer submits a HYDROXYPROPYLMETHYLCELLULOSE CEP (COS) as part of the market authorization procedure, and it takes on the role of a HYDROXYPROPYLMETHYLCELLULOSE CEP holder for the record. Additionally, the data presented in the HYDROXYPROPYLMETHYLCELLULOSE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the HYDROXYPROPYLMETHYLCELLULOSE DMF.
A HYDROXYPROPYLMETHYLCELLULOSE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. HYDROXYPROPYLMETHYLCELLULOSE CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of HYDROXYPROPYLMETHYLCELLULOSE suppliers with CEP (COS) on PharmaCompass.
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