Curia- A partner for the pharma and biotech industries to improve patient outcomes & quality of life.

Reset all filters
01 1CURIA SPAIN S.A.U. Boecillo ES
02 1INDUSTRIALE CHIMICA S.R.L. Saronno IT
Reset all filters
01 2Etonogestrel
Reset all filters
01 1Italy
02 1U.S.A
Reset all filters
01 2Valid
Curia- A partner for the pharma and biotech industries to improve patient outcomes & quality of life.
Curia- A partner for the pharma and biotech industries to improve patient outcomes & quality of life.
Certificate Number : CEP 2025-093 - Rev 01
Status : Valid
Issue Date : 2025-10-16
Type : Chemical
Substance Number : 3049
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

Certificate Number : CEP 2025-195 - Rev 00
Status : Valid
Issue Date : 2025-11-10
Type : Chemical
Substance Number : 3049

92
PharmaCompass offers a list of Etonogestrel 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 Etonogestrel manufacturer or Etonogestrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etonogestrel manufacturer or Etonogestrel supplier.
PharmaCompass also assists you with knowing the Etonogestrel API Price utilized in the formulation of products. Etonogestrel API Price is not always fixed or binding as the Etonogestrel Price is obtained through a variety of data sources. The Etonogestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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, COA and API Price 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, COA and API Price 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.
click here to find a list of Implanon suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Implanon
Get in contact with the supplier of your choice: