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Status : Withdrawn by Holder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 :
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.
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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 Ossopan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ossopan, including repackagers and relabelers. The FDA regulates Ossopan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ossopan 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 Ossopan supplier is an individual or a company that provides Ossopan active pharmaceutical ingredient (API) or Ossopan finished formulations upon request. The Ossopan suppliers may include Ossopan API manufacturers, exporters, distributors and traders.
click here to find a list of Ossopan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ossopan CEP of the European Pharmacopoeia monograph is often referred to as a Ossopan Certificate of Suitability (COS). The purpose of a Ossopan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ossopan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ossopan to their clients by showing that a Ossopan CEP has been issued for it. The manufacturer submits a Ossopan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ossopan CEP holder for the record. Additionally, the data presented in the Ossopan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ossopan DMF.
A Ossopan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ossopan 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 Ossopan suppliers with CEP (COS) on PharmaCompass.
