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
A Hyaluronidase manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyaluronidase, including repackagers and relabelers. The FDA regulates Hyaluronidase manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyaluronidase API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Hyaluronidase manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hyaluronidase supplier is an individual or a company that provides Hyaluronidase active pharmaceutical ingredient (API) or Hyaluronidase finished formulations upon request. The Hyaluronidase suppliers may include Hyaluronidase API manufacturers, exporters, distributors and traders.
click here to find a list of Hyaluronidase suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hyaluronidase CEP of the European Pharmacopoeia monograph is often referred to as a Hyaluronidase Certificate of Suitability (COS). The purpose of a Hyaluronidase CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hyaluronidase EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hyaluronidase to their clients by showing that a Hyaluronidase CEP has been issued for it. The manufacturer submits a Hyaluronidase CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hyaluronidase CEP holder for the record. Additionally, the data presented in the Hyaluronidase CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hyaluronidase DMF.
A Hyaluronidase CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hyaluronidase 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 Hyaluronidase suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering Hyaluronidase
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
