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