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