Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Listed Suppliers
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API
0
FDF
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS0
EDQM
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USP
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JP
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Others
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US Patents
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US Exclusivities
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Health Canada Patents
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 1mCi/ML
USFDA APPLICATION NUMBER - 17806
DOSAGE - INJECTABLE;INTRAVENOUS - 2mCi/ML
USFDA APPLICATION NUMBER - 17806
DOSAGE - INJECTABLE;INJECTION - 1mCi/ML
USFDA APPLICATION NUMBER - 18110
DOSAGE - INJECTABLE;INJECTION - 1mCi/ML
USFDA APPLICATION NUMBER - 18150
Related Excipient Companies
Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Parenteral
Topical
Solubilizers
ABOUT THIS PAGE
A Thallium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thallium Chloride, including repackagers and relabelers. The FDA regulates Thallium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thallium Chloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Thallium Chloride supplier is an individual or a company that provides Thallium Chloride active pharmaceutical ingredient (API) or Thallium Chloride finished formulations upon request. The Thallium Chloride suppliers may include Thallium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Thallium Chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Thallium Chloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Thallium Chloride active pharmaceutical ingredient (API) in detail. Different forms of Thallium Chloride DMFs exist exist since differing nations have different regulations, such as Thallium Chloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Thallium Chloride DMF submitted to regulatory agencies in the US is known as a USDMF. Thallium Chloride USDMF includes data on Thallium Chloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Thallium Chloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Thallium Chloride suppliers with USDMF on PharmaCompass.
Thallium Chloride 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 Thallium Chloride 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 Thallium Chloride GMP manufacturer or Thallium Chloride GMP API supplier for your needs.
A Thallium Chloride CoA (Certificate of Analysis) is a formal document that attests to Thallium Chloride's compliance with Thallium Chloride specifications and serves as a tool for batch-level quality control.
Thallium Chloride CoA mostly includes findings from lab analyses of a specific batch. For each Thallium Chloride 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.
Thallium Chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Thallium Chloride EP), Thallium Chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Thallium Chloride USP).
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