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PharmaCompass offers a list of Cycloserine 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 Cycloserine manufacturer or Cycloserine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cycloserine manufacturer or Cycloserine supplier.
PharmaCompass also assists you with knowing the Cycloserine API Price utilized in the formulation of products. Cycloserine API Price is not always fixed or binding as the Cycloserine Price is obtained through a variety of data sources. The Cycloserine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cycloserine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cycloserine, including repackagers and relabelers. The FDA regulates Cycloserine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cycloserine 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 Cycloserine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cycloserine supplier is an individual or a company that provides Cycloserine active pharmaceutical ingredient (API) or Cycloserine finished formulations upon request. The Cycloserine suppliers may include Cycloserine API manufacturers, exporters, distributors and traders.
click here to find a list of Cycloserine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cycloserine DMF (Drug Master File) is a document detailing the whole manufacturing process of Cycloserine active pharmaceutical ingredient (API) in detail. Different forms of Cycloserine DMFs exist exist since differing nations have different regulations, such as Cycloserine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cycloserine DMF submitted to regulatory agencies in the US is known as a USDMF. Cycloserine USDMF includes data on Cycloserine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cycloserine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cycloserine 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 Cycloserine Drug Master File in Korea (Cycloserine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cycloserine. The MFDS reviews the Cycloserine KDMF as part of the drug registration process and uses the information provided in the Cycloserine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cycloserine 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 Cycloserine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cycloserine suppliers with KDMF on PharmaCompass.
A Cycloserine written confirmation (Cycloserine WC) is an official document issued by a regulatory agency to a Cycloserine manufacturer, verifying that the manufacturing facility of a Cycloserine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cycloserine APIs or Cycloserine finished pharmaceutical products to another nation, regulatory agencies frequently require a Cycloserine WC (written confirmation) as part of the regulatory process.
click here to find a list of Cycloserine 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 Cycloserine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cycloserine 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 Cycloserine 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 Cycloserine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cycloserine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cycloserine suppliers with NDC on PharmaCompass.
Cycloserine 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 Cycloserine 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 Cycloserine GMP manufacturer or Cycloserine GMP API supplier for your needs.
A Cycloserine CoA (Certificate of Analysis) is a formal document that attests to Cycloserine's compliance with Cycloserine specifications and serves as a tool for batch-level quality control.
Cycloserine CoA mostly includes findings from lab analyses of a specific batch. For each Cycloserine 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.
Cycloserine may be tested according to a variety of international standards, such as European Pharmacopoeia (Cycloserine EP), Cycloserine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cycloserine USP).
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