01 1BBI ENZYMES SA (PTY) LTD Cape Town ZA
02 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
03 1Sigma-Aldrich Corporation Saint Louis US
01 1Hyaluronidase
02 1Hyaluronidase, Product codes: 081231, 081236, 081239, 081240, 081242, 081244, 081245, 081246 and 081247
03 1Hyaluronidase, Type VIII, (Product Number H2032)
01 1Italy
02 1South Africa
03 1U.S.A
01 1Expired
02 1Suspended by EDQM GMP non-compliance
03 1Valid
Hyaluronidase, Product Codes: 081231, 081236, 08...
Certificate Number : R1-CEP 2001-085 - Rev 02
Status : Valid
Issue Date : 2010-06-01
Type : TSE
Substance Number : 912
Certificate Number : R1-CEP 2001-068 - Rev 00
Status : Suspended by EDQM GMP non-compliance
Issue Date : 2007-04-04
Type : TSE
Substance Number : 912
Hyaluronidase, Type VIII, (Product Number H2032)
Certificate Number : R0-CEP 2001-364 - Rev 01
Status : Expired
Issue Date : 2005-03-18
Type : TSE
Substance Number : 912
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PharmaCompass offers a list of Hyaluronidase 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 Hyaluronidase manufacturer or Hyaluronidase supplier for your needs.
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PharmaCompass also assists you with knowing the Hyaluronidase API Price utilized in the formulation of products. Hyaluronidase API Price is not always fixed or binding as the Hyaluronidase Price is obtained through a variety of data sources. The Hyaluronidase Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A WYDASE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of WYDASE, including repackagers and relabelers. The FDA regulates WYDASE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. WYDASE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A WYDASE supplier is an individual or a company that provides WYDASE active pharmaceutical ingredient (API) or WYDASE finished formulations upon request. The WYDASE suppliers may include WYDASE API manufacturers, exporters, distributors and traders.
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A WYDASE CEP of the European Pharmacopoeia monograph is often referred to as a WYDASE Certificate of Suitability (COS). The purpose of a WYDASE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of WYDASE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of WYDASE to their clients by showing that a WYDASE CEP has been issued for it. The manufacturer submits a WYDASE CEP (COS) as part of the market authorization procedure, and it takes on the role of a WYDASE CEP holder for the record. Additionally, the data presented in the WYDASE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the WYDASE DMF.
A WYDASE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. WYDASE 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 WYDASE suppliers with CEP (COS) on PharmaCompass.
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