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01 1PIERRE FABRE MEDICAMENT Gaillac FR
02 1Pierre Fabre Medicament Gaillac FR
03 1Pierre Fabre Santé - Plantes & Industrie Gaillac FR
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01 1MicroCrystalline Hydroxyapatite Compound
02 2Ossein Hydroxyapatite Compound
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01 3France
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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Status : Withdrawn by Holder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 :
15
PharmaCompass offers a list of HYDROXYPROPYLMETHYLCELLULOSE API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right HYDROXYPROPYLMETHYLCELLULOSE manufacturer or HYDROXYPROPYLMETHYLCELLULOSE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred HYDROXYPROPYLMETHYLCELLULOSE manufacturer or HYDROXYPROPYLMETHYLCELLULOSE supplier.
PharmaCompass also assists you with knowing the HYDROXYPROPYLMETHYLCELLULOSE API Price utilized in the formulation of products. HYDROXYPROPYLMETHYLCELLULOSE API Price is not always fixed or binding as the HYDROXYPROPYLMETHYLCELLULOSE Price is obtained through a variety of data sources. The HYDROXYPROPYLMETHYLCELLULOSE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Calcium Hydroxyapatite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Hydroxyapatite, including repackagers and relabelers. The FDA regulates Calcium Hydroxyapatite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Hydroxyapatite 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 Calcium Hydroxyapatite supplier is an individual or a company that provides Calcium Hydroxyapatite active pharmaceutical ingredient (API) or Calcium Hydroxyapatite finished formulations upon request. The Calcium Hydroxyapatite suppliers may include Calcium Hydroxyapatite API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Hydroxyapatite suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Calcium Hydroxyapatite CEP of the European Pharmacopoeia monograph is often referred to as a Calcium Hydroxyapatite Certificate of Suitability (COS). The purpose of a Calcium Hydroxyapatite CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Calcium Hydroxyapatite EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Calcium Hydroxyapatite to their clients by showing that a Calcium Hydroxyapatite CEP has been issued for it. The manufacturer submits a Calcium Hydroxyapatite CEP (COS) as part of the market authorization procedure, and it takes on the role of a Calcium Hydroxyapatite CEP holder for the record. Additionally, the data presented in the Calcium Hydroxyapatite CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Calcium Hydroxyapatite DMF.
A Calcium Hydroxyapatite CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Calcium Hydroxyapatite 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 Calcium Hydroxyapatite suppliers with CEP (COS) on PharmaCompass.
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