Suanfarma, at the Core of a Better Life.
01 1CIPAN - COMPANHIA INDUSTRIAL PRODUTORA DE ANTIBIOTICOS, S.A. Castanheira Do Ribatejo PT
02 1KOPRAN RESEARCH LABORATORIES LIMITED Mumbai IN
03 2OLON S.P.A. Rodano IT
01 3Lymecycline
02 1Lymecycline, Type 2
01 1India
02 2Italy
03 1Spain
01 4Valid
Suanfarma, at the Core of a Better Life.
Suanfarma, at the Core of a Better Life.
Certificate Number : R1-CEP 2010-239 - Rev 02
Status : Valid
Issue Date : 2023-02-09
Type : Chemical
Substance Number : 1654
Certificate Number : CEP 2020-040 - Rev 01
Status : Valid
Issue Date : 2024-12-18
Type : Chemical
Substance Number : 1654
Certificate Number : R1-CEP 2016-186 - Rev 01
Status : Valid
Issue Date : 2023-04-26
Type : Chemical
Substance Number : 1654
Certificate Number : R0-CEP 2023-172 - Rev 00
Status : Valid
Issue Date : 2023-08-09
Type : Chemical
Substance Number : 1654
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A Tetraciclina-L-metilenlisina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetraciclina-L-metilenlisina, including repackagers and relabelers. The FDA regulates Tetraciclina-L-metilenlisina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetraciclina-L-metilenlisina 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 Tetraciclina-L-metilenlisina supplier is an individual or a company that provides Tetraciclina-L-metilenlisina active pharmaceutical ingredient (API) or Tetraciclina-L-metilenlisina finished formulations upon request. The Tetraciclina-L-metilenlisina suppliers may include Tetraciclina-L-metilenlisina API manufacturers, exporters, distributors and traders.
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A Tetraciclina-L-metilenlisina CEP of the European Pharmacopoeia monograph is often referred to as a Tetraciclina-L-metilenlisina Certificate of Suitability (COS). The purpose of a Tetraciclina-L-metilenlisina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tetraciclina-L-metilenlisina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tetraciclina-L-metilenlisina to their clients by showing that a Tetraciclina-L-metilenlisina CEP has been issued for it. The manufacturer submits a Tetraciclina-L-metilenlisina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tetraciclina-L-metilenlisina CEP holder for the record. Additionally, the data presented in the Tetraciclina-L-metilenlisina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tetraciclina-L-metilenlisina DMF.
A Tetraciclina-L-metilenlisina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tetraciclina-L-metilenlisina CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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