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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 5mCi/0.5ML
USFDA APPLICATION NUMBER - 19841
DOSAGE - INJECTABLE;INJECTION - 2mCi/0.2ML
USFDA APPLICATION NUMBER - 19862
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ABOUT THIS PAGE
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PharmaCompass offers a list of Indium Trichloride 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 Indium Trichloride manufacturer or Indium Trichloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indium Trichloride manufacturer or Indium Trichloride supplier.
PharmaCompass also assists you with knowing the Indium Trichloride API Price utilized in the formulation of products. Indium Trichloride API Price is not always fixed or binding as the Indium Trichloride Price is obtained through a variety of data sources. The Indium Trichloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Indium Trichloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indium Trichloride, including repackagers and relabelers. The FDA regulates Indium Trichloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indium Trichloride 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 Indium Trichloride supplier is an individual or a company that provides Indium Trichloride active pharmaceutical ingredient (API) or Indium Trichloride finished formulations upon request. The Indium Trichloride suppliers may include Indium Trichloride API manufacturers, exporters, distributors and traders.
click here to find a list of Indium Trichloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Indium Trichloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Indium Trichloride active pharmaceutical ingredient (API) in detail. Different forms of Indium Trichloride DMFs exist exist since differing nations have different regulations, such as Indium Trichloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Indium Trichloride DMF submitted to regulatory agencies in the US is known as a USDMF. Indium Trichloride USDMF includes data on Indium Trichloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Indium Trichloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Indium Trichloride suppliers with USDMF on PharmaCompass.
Indium Trichloride 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 Indium Trichloride 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 Indium Trichloride GMP manufacturer or Indium Trichloride GMP API supplier for your needs.
A Indium Trichloride CoA (Certificate of Analysis) is a formal document that attests to Indium Trichloride's compliance with Indium Trichloride specifications and serves as a tool for batch-level quality control.
Indium Trichloride CoA mostly includes findings from lab analyses of a specific batch. For each Indium Trichloride 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.
Indium Trichloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Indium Trichloride EP), Indium Trichloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Indium Trichloride USP).
