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API SUPPLIERS
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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Minakem
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Sulfasalazine 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 Sulfasalazine manufacturer or Sulfasalazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfasalazine manufacturer or Sulfasalazine supplier.
PharmaCompass also assists you with knowing the Sulfasalazine API Price utilized in the formulation of products. Sulfasalazine API Price is not always fixed or binding as the Sulfasalazine Price is obtained through a variety of data sources. The Sulfasalazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Disalazin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disalazin, including repackagers and relabelers. The FDA regulates Disalazin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disalazin 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 Disalazin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disalazin supplier is an individual or a company that provides Disalazin active pharmaceutical ingredient (API) or Disalazin finished formulations upon request. The Disalazin suppliers may include Disalazin API manufacturers, exporters, distributors and traders.
click here to find a list of Disalazin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disalazin DMF (Drug Master File) is a document detailing the whole manufacturing process of Disalazin active pharmaceutical ingredient (API) in detail. Different forms of Disalazin DMFs exist exist since differing nations have different regulations, such as Disalazin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Disalazin DMF submitted to regulatory agencies in the US is known as a USDMF. Disalazin USDMF includes data on Disalazin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Disalazin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Disalazin 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 Disalazin Drug Master File in Japan (Disalazin JDMF) empowers Disalazin 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 Disalazin JDMF during the approval evaluation for pharmaceutical products. At the time of Disalazin 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 Disalazin suppliers with JDMF 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 Disalazin Drug Master File in Korea (Disalazin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Disalazin. The MFDS reviews the Disalazin KDMF as part of the drug registration process and uses the information provided in the Disalazin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Disalazin 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 Disalazin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Disalazin suppliers with KDMF on PharmaCompass.
A Disalazin CEP of the European Pharmacopoeia monograph is often referred to as a Disalazin Certificate of Suitability (COS). The purpose of a Disalazin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Disalazin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Disalazin to their clients by showing that a Disalazin CEP has been issued for it. The manufacturer submits a Disalazin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Disalazin CEP holder for the record. Additionally, the data presented in the Disalazin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Disalazin DMF.
A Disalazin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Disalazin 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 Disalazin suppliers with CEP (COS) on PharmaCompass.
A Disalazin written confirmation (Disalazin WC) is an official document issued by a regulatory agency to a Disalazin manufacturer, verifying that the manufacturing facility of a Disalazin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Disalazin APIs or Disalazin finished pharmaceutical products to another nation, regulatory agencies frequently require a Disalazin WC (written confirmation) as part of the regulatory process.
click here to find a list of Disalazin 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 Disalazin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Disalazin 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 Disalazin 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 Disalazin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Disalazin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Disalazin suppliers with NDC on PharmaCompass.
Disalazin 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 Disalazin 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 Disalazin GMP manufacturer or Disalazin GMP API supplier for your needs.
A Disalazin CoA (Certificate of Analysis) is a formal document that attests to Disalazin's compliance with Disalazin specifications and serves as a tool for batch-level quality control.
Disalazin CoA mostly includes findings from lab analyses of a specific batch. For each Disalazin 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.
Disalazin may be tested according to a variety of international standards, such as European Pharmacopoeia (Disalazin EP), Disalazin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Disalazin USP).
