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