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