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