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API SUPPLIERS
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USDMF
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Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
About the Company : Octavius Pharma is a global leader in Directly Compressible Granules with over 40 years of experience in Formulation development, manufacturing and commercialization. It offers a w...
Suanfarma, at the Core of a Better Life.
About the Company : Suanfarma founded in 1993, is a B2B life science partner committed to health advancement by developing, manufacturing, & distributing high-quality APIs for the pharmaceutical indus...
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
About the Company : Since its inception in 2003, Seqens has evolved into a global leader in pharmaceutical solutions and specialty ingredients. With a strong focus on customer support, Seqens assists ...
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
About the Company : Egis is a member of the Servier Group. Egis’ products are manufactured at 3 production sites in Hungary, which are certified by EMA,FDA, ANVISA, PMDA ,KFDA. Egis sells its produc...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
Mesochem is focused on incessant innovation along with the R&D of new APIs.
About the Company : Beijing Mesochem Technology Co. Ltd., which is located in the national economic and technological development area of Yizhuang, China, manufactures pharmaceutical chemicals, fine c...
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PharmaCompass offers a list of Clomiphene Citrate 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 Clomiphene Citrate manufacturer or Clomiphene Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clomiphene Citrate manufacturer or Clomiphene Citrate supplier.
PharmaCompass also assists you with knowing the Clomiphene Citrate API Price utilized in the formulation of products. Clomiphene Citrate API Price is not always fixed or binding as the Clomiphene Citrate Price is obtained through a variety of data sources. The Clomiphene Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clomiphene Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clomiphene Citrate, including repackagers and relabelers. The FDA regulates Clomiphene Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clomiphene Citrate 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 Clomiphene Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clomiphene Citrate supplier is an individual or a company that provides Clomiphene Citrate active pharmaceutical ingredient (API) or Clomiphene Citrate finished formulations upon request. The Clomiphene Citrate suppliers may include Clomiphene Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Clomiphene Citrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clomiphene Citrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Clomiphene Citrate active pharmaceutical ingredient (API) in detail. Different forms of Clomiphene Citrate DMFs exist exist since differing nations have different regulations, such as Clomiphene Citrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Clomiphene Citrate DMF submitted to regulatory agencies in the US is known as a USDMF. Clomiphene Citrate USDMF includes data on Clomiphene Citrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Clomiphene Citrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Clomiphene Citrate suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Clomiphene Citrate Drug Master File in Japan (Clomiphene Citrate JDMF) empowers Clomiphene Citrate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Clomiphene Citrate JDMF during the approval evaluation for pharmaceutical products. At the time of Clomiphene Citrate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Clomiphene Citrate suppliers with JDMF on PharmaCompass.
A Clomiphene Citrate CEP of the European Pharmacopoeia monograph is often referred to as a Clomiphene Citrate Certificate of Suitability (COS). The purpose of a Clomiphene Citrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clomiphene Citrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clomiphene Citrate to their clients by showing that a Clomiphene Citrate CEP has been issued for it. The manufacturer submits a Clomiphene Citrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clomiphene Citrate CEP holder for the record. Additionally, the data presented in the Clomiphene Citrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clomiphene Citrate DMF.
A Clomiphene Citrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clomiphene Citrate 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 Clomiphene Citrate suppliers with CEP (COS) on PharmaCompass.
A Clomiphene Citrate written confirmation (Clomiphene Citrate WC) is an official document issued by a regulatory agency to a Clomiphene Citrate manufacturer, verifying that the manufacturing facility of a Clomiphene Citrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clomiphene Citrate APIs or Clomiphene Citrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Clomiphene Citrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Clomiphene Citrate suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Clomiphene Citrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Clomiphene Citrate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Clomiphene Citrate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Clomiphene Citrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Clomiphene Citrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Clomiphene Citrate suppliers with NDC on PharmaCompass.
Clomiphene Citrate Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Clomiphene Citrate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Clomiphene Citrate GMP manufacturer or Clomiphene Citrate GMP API supplier for your needs.
A Clomiphene Citrate CoA (Certificate of Analysis) is a formal document that attests to Clomiphene Citrate's compliance with Clomiphene Citrate specifications and serves as a tool for batch-level quality control.
Clomiphene Citrate CoA mostly includes findings from lab analyses of a specific batch. For each Clomiphene Citrate CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Clomiphene Citrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Clomiphene Citrate EP), Clomiphene Citrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Clomiphene Citrate USP).
