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PharmaCompass offers a list of Intermedine 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 Intermedine manufacturer or Intermedine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Intermedine manufacturer or Intermedine supplier.
PharmaCompass also assists you with knowing the Intermedine API Price utilized in the formulation of products. Intermedine API Price is not always fixed or binding as the Intermedine Price is obtained through a variety of data sources. The Intermedine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Intermedine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Intermedine, including repackagers and relabelers. The FDA regulates Intermedine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Intermedine 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 Intermedine supplier is an individual or a company that provides Intermedine active pharmaceutical ingredient (API) or Intermedine finished formulations upon request. The Intermedine suppliers may include Intermedine API manufacturers, exporters, distributors and traders.
Intermedine 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 Intermedine 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 Intermedine GMP manufacturer or Intermedine GMP API supplier for your needs.
A Intermedine CoA (Certificate of Analysis) is a formal document that attests to Intermedine's compliance with Intermedine specifications and serves as a tool for batch-level quality control.
Intermedine CoA mostly includes findings from lab analyses of a specific batch. For each Intermedine 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.
Intermedine may be tested according to a variety of international standards, such as European Pharmacopoeia (Intermedine EP), Intermedine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Intermedine USP).
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