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