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