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API SUPPLIERS
Inke S.A: APIs manufacturing plant.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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USDMF
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Inke S.A: APIs manufacturing plant.
About the Company : Inke S.A., is focused since 1980 in the development and manufacture of the highest quality Active Pharmaceutical Ingredients (APIs) with complex synthesis processes for diverse the...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
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Drugs in Development
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PharmaCompass offers a list of Prasugrel 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 Prasugrel manufacturer or Prasugrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prasugrel manufacturer or Prasugrel supplier.
PharmaCompass also assists you with knowing the Prasugrel API Price utilized in the formulation of products. Prasugrel API Price is not always fixed or binding as the Prasugrel Price is obtained through a variety of data sources. The Prasugrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Effient manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effient, including repackagers and relabelers. The FDA regulates Effient manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effient 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 Effient manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Effient supplier is an individual or a company that provides Effient active pharmaceutical ingredient (API) or Effient finished formulations upon request. The Effient suppliers may include Effient API manufacturers, exporters, distributors and traders.
click here to find a list of Effient suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Effient DMF (Drug Master File) is a document detailing the whole manufacturing process of Effient active pharmaceutical ingredient (API) in detail. Different forms of Effient DMFs exist exist since differing nations have different regulations, such as Effient USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Effient DMF submitted to regulatory agencies in the US is known as a USDMF. Effient USDMF includes data on Effient's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Effient USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Effient suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Effient Drug Master File in Korea (Effient KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Effient. The MFDS reviews the Effient KDMF as part of the drug registration process and uses the information provided in the Effient KDMF to evaluate the safety and efficacy of the drug.
After submitting a Effient KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Effient API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Effient suppliers with KDMF on PharmaCompass.
A Effient written confirmation (Effient WC) is an official document issued by a regulatory agency to a Effient manufacturer, verifying that the manufacturing facility of a Effient active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Effient APIs or Effient finished pharmaceutical products to another nation, regulatory agencies frequently require a Effient WC (written confirmation) as part of the regulatory process.
click here to find a list of Effient 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 Effient as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Effient 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 Effient 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 Effient and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Effient NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Effient suppliers with NDC on PharmaCompass.
Effient 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 Effient 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 Effient GMP manufacturer or Effient GMP API supplier for your needs.
A Effient CoA (Certificate of Analysis) is a formal document that attests to Effient's compliance with Effient specifications and serves as a tool for batch-level quality control.
Effient CoA mostly includes findings from lab analyses of a specific batch. For each Effient 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.
Effient may be tested according to a variety of international standards, such as European Pharmacopoeia (Effient EP), Effient JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Effient USP).
