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