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API SUPPLIERS
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USDMF
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Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
About the Company : Symbiotec, a leading API manufacturing company based in Indore, Central India, specializes in Cortico-Steroids and Steroid-Hormone APIs. Since 1995, their focus on R&D, sustainable...
Zeon Pharma is a manufacturer and supplier of APIs & Intermediates.
About the Company : Zeon Pharma Industries India Pvt ltd is an ISO & GMP certified manufacturer of Bulk drugs & Intermediate and also supplies our associate manufacturing plant API / Semi finish form...
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API Imports and Exports
FDF Dossiers
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Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Serratiopeptidase
Dosage Form : Gastro Resistant Table...
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Serratiopeptidase
Dosage Form : Gastro Resistant Table...
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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PharmaCompass offers a list of Serratiopeptidase 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 Serratiopeptidase manufacturer or Serratiopeptidase supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Serratiopeptidase manufacturer or Serratiopeptidase supplier.
PharmaCompass also assists you with knowing the Serratiopeptidase API Price utilized in the formulation of products. Serratiopeptidase API Price is not always fixed or binding as the Serratiopeptidase Price is obtained through a variety of data sources. The Serratiopeptidase Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Danzen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Danzen, including repackagers and relabelers. The FDA regulates Danzen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Danzen 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 Danzen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Danzen supplier is an individual or a company that provides Danzen active pharmaceutical ingredient (API) or Danzen finished formulations upon request. The Danzen suppliers may include Danzen API manufacturers, exporters, distributors and traders.
click here to find a list of Danzen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Danzen DMF (Drug Master File) is a document detailing the whole manufacturing process of Danzen active pharmaceutical ingredient (API) in detail. Different forms of Danzen DMFs exist exist since differing nations have different regulations, such as Danzen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Danzen DMF submitted to regulatory agencies in the US is known as a USDMF. Danzen USDMF includes data on Danzen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Danzen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Danzen suppliers with USDMF on PharmaCompass.
Danzen 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 Danzen 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 Danzen GMP manufacturer or Danzen GMP API supplier for your needs.
A Danzen CoA (Certificate of Analysis) is a formal document that attests to Danzen's compliance with Danzen specifications and serves as a tool for batch-level quality control.
Danzen CoA mostly includes findings from lab analyses of a specific batch. For each Danzen 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.
Danzen may be tested according to a variety of international standards, such as European Pharmacopoeia (Danzen EP), Danzen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Danzen USP).
