01 1CHEMO BIOSYNTHESIS S.R.L. Corana IT
02 2HEBEI VEYONG PHARMACEUTICAL CO., LTD. Shijiazhuang CN
03 1Hovione PharmaScience Limited Taipa MO
04 1Merck & Co Inc Whitehouse Station US
05 1North China Pharmaceutical Group Aino Co., Ltd. Shijiazhuang CN
06 1RICHBERYL BIOTECH CO., LTD. OF RAOYANG COUNTY Hengshui CN
07 1Shandong Qilu King-Phar Pharmaceutical Co., Ltd Pingyin CN
08 1ZHEJIANG APELOA KANGYU PHARMACEUTICAL CO., LTD. Hengdian CN
09 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
01 9Ivermectin
02 1Ivermectin, Process II
01 7China
02 1Italy
03 1Portugal
04 1U.S.A
01 2Expired
02 7Valid
03 1Withdrawn by Holder
Certificate Number : CEP 2021-382 - Rev 00
Status : Valid
Issue Date : 2024-08-02
Type : Chemical
Substance Number : 1336
Certificate Number : R0-CEP 2021-477 - Rev 00
Status : Valid
Issue Date : 2022-04-22
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 2008-104 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2020-06-08
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 1998-138 - Rev 05
Status : Valid
Issue Date : 2020-02-28
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 2001-146 - Rev 01
Status : Valid
Issue Date : 2008-11-27
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 2004-070 - Rev 01
Status : Valid
Issue Date : 2011-08-02
Type : Chemical
Substance Number : 1336
Certificate Number : R0-CEP 2010-123 - Rev 00
Status : Expired
Issue Date : 2011-10-25
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 2001-077 - Rev 01
Status : Valid
Issue Date : 2017-10-16
Type : Chemical
Substance Number : 1336
Certificate Number : R0-CEP 2006-008 - Rev 01
Status : Expired
Issue Date : 2010-06-17
Type : Chemical
Substance Number : 1336
Certificate Number : R1-CEP 1999-176 - Rev 05
Status : Valid
Issue Date : 2021-03-31
Type : Chemical
Substance Number : 1336
A Ivermectin B1a manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivermectin B1a, including repackagers and relabelers. The FDA regulates Ivermectin B1a manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivermectin B1a 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 Ivermectin B1a supplier is an individual or a company that provides Ivermectin B1a active pharmaceutical ingredient (API) or Ivermectin B1a finished formulations upon request. The Ivermectin B1a suppliers may include Ivermectin B1a API manufacturers, exporters, distributors and traders.
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A Ivermectin B1a CEP of the European Pharmacopoeia monograph is often referred to as a Ivermectin B1a Certificate of Suitability (COS). The purpose of a Ivermectin B1a CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ivermectin B1a EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ivermectin B1a to their clients by showing that a Ivermectin B1a CEP has been issued for it. The manufacturer submits a Ivermectin B1a CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ivermectin B1a CEP holder for the record. Additionally, the data presented in the Ivermectin B1a CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ivermectin B1a DMF.
A Ivermectin B1a CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ivermectin B1a 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 Ivermectin B1a suppliers with CEP (COS) on PharmaCompass.
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