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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
A Homoharringtonine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homoharringtonine, including repackagers and relabelers. The FDA regulates Homoharringtonine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homoharringtonine 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 Homoharringtonine supplier is an individual or a company that provides Homoharringtonine active pharmaceutical ingredient (API) or Homoharringtonine finished formulations upon request. The Homoharringtonine suppliers may include Homoharringtonine API manufacturers, exporters, distributors and traders.
click here to find a list of Homoharringtonine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Homoharringtonine DMF (Drug Master File) is a document detailing the whole manufacturing process of Homoharringtonine active pharmaceutical ingredient (API) in detail. Different forms of Homoharringtonine DMFs exist exist since differing nations have different regulations, such as Homoharringtonine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Homoharringtonine DMF submitted to regulatory agencies in the US is known as a USDMF. Homoharringtonine USDMF includes data on Homoharringtonine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Homoharringtonine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Homoharringtonine suppliers with USDMF 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 Homoharringtonine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Homoharringtonine 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 Homoharringtonine 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 Homoharringtonine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Homoharringtonine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Homoharringtonine suppliers with NDC on PharmaCompass.
Homoharringtonine 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 Homoharringtonine 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 Homoharringtonine GMP manufacturer or Homoharringtonine GMP API supplier for your needs.
A Homoharringtonine CoA (Certificate of Analysis) is a formal document that attests to Homoharringtonine's compliance with Homoharringtonine specifications and serves as a tool for batch-level quality control.
Homoharringtonine CoA mostly includes findings from lab analyses of a specific batch. For each Homoharringtonine 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.
Homoharringtonine may be tested according to a variety of international standards, such as European Pharmacopoeia (Homoharringtonine EP), Homoharringtonine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Homoharringtonine USP).
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