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Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
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USDMF
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Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
About the Company : Established in 2004 and headquartered in Hangzhou, Hengkang established multiple factories, research and sales centers in Zhejiang, Shandong, and Henan. With facilities conforming ...
Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
About the Company : Bioquim is a European company specializing in bulk oral & sterile APIs for the pharmaceutical industry. With over 40 years of experience, we offer high-quality corticosteroids, pep...
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PharmaCompass offers a list of Ademetionine 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 Ademetionine manufacturer or Ademetionine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ademetionine manufacturer or Ademetionine supplier.
PharmaCompass also assists you with knowing the Ademetionine API Price utilized in the formulation of products. Ademetionine API Price is not always fixed or binding as the Ademetionine Price is obtained through a variety of data sources. The Ademetionine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Samyr manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Samyr, including repackagers and relabelers. The FDA regulates Samyr manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Samyr 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 Samyr manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Samyr supplier is an individual or a company that provides Samyr active pharmaceutical ingredient (API) or Samyr finished formulations upon request. The Samyr suppliers may include Samyr API manufacturers, exporters, distributors and traders.
click here to find a list of Samyr suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Samyr DMF (Drug Master File) is a document detailing the whole manufacturing process of Samyr active pharmaceutical ingredient (API) in detail. Different forms of Samyr DMFs exist exist since differing nations have different regulations, such as Samyr USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Samyr DMF submitted to regulatory agencies in the US is known as a USDMF. Samyr USDMF includes data on Samyr's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Samyr USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Samyr suppliers with USDMF on PharmaCompass.
Samyr 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 Samyr 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 Samyr GMP manufacturer or Samyr GMP API supplier for your needs.
A Samyr CoA (Certificate of Analysis) is a formal document that attests to Samyr's compliance with Samyr specifications and serves as a tool for batch-level quality control.
Samyr CoA mostly includes findings from lab analyses of a specific batch. For each Samyr 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.
Samyr may be tested according to a variety of international standards, such as European Pharmacopoeia (Samyr EP), Samyr JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Samyr USP).
