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