Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
01 1CURIA SPAIN S.A.U. Boecillo ES
02 1INDUSTRIALE CHIMICA S.R.L. Saronno IT
01 2Etonogestrel
01 1Italy
02 1U.S.A
01 2Valid
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Certificate Number : CEP 2025-093 - Rev 01
Status : Valid
Issue Date : 2025-10-16
Type : Chemical
Substance Number : 3049
Certificate Number : CEP 2025-195 - Rev 00
Status : Valid
Issue Date : 2025-11-10
Type : Chemical
Substance Number : 3049
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A Implanon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Implanon, including repackagers and relabelers. The FDA regulates Implanon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Implanon 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 Implanon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Implanon supplier is an individual or a company that provides Implanon active pharmaceutical ingredient (API) or Implanon finished formulations upon request. The Implanon suppliers may include Implanon API manufacturers, exporters, distributors and traders.
click here to find a list of Implanon suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Implanon CEP of the European Pharmacopoeia monograph is often referred to as a Implanon Certificate of Suitability (COS). The purpose of a Implanon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Implanon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Implanon to their clients by showing that a Implanon CEP has been issued for it. The manufacturer submits a Implanon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Implanon CEP holder for the record. Additionally, the data presented in the Implanon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Implanon DMF.
A Implanon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Implanon 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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