Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
API
0
FDF
0
Europe
0
Canada
0
Australia
0
South Africa
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
ABOUT THIS PAGE
90
PharmaCompass offers a list of Dezocine 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 Dezocine manufacturer or Dezocine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dezocine manufacturer or Dezocine supplier.
PharmaCompass also assists you with knowing the Dezocine API Price utilized in the formulation of products. Dezocine API Price is not always fixed or binding as the Dezocine Price is obtained through a variety of data sources. The Dezocine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dezocine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dezocine, including repackagers and relabelers. The FDA regulates Dezocine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dezocine 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 Dezocine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dezocine supplier is an individual or a company that provides Dezocine active pharmaceutical ingredient (API) or Dezocine finished formulations upon request. The Dezocine suppliers may include Dezocine API manufacturers, exporters, distributors and traders.
click here to find a list of Dezocine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dezocine DMF (Drug Master File) is a document detailing the whole manufacturing process of Dezocine active pharmaceutical ingredient (API) in detail. Different forms of Dezocine DMFs exist exist since differing nations have different regulations, such as Dezocine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dezocine DMF submitted to regulatory agencies in the US is known as a USDMF. Dezocine USDMF includes data on Dezocine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dezocine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dezocine suppliers with USDMF on PharmaCompass.
Dezocine 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 Dezocine 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 Dezocine GMP manufacturer or Dezocine GMP API supplier for your needs.
A Dezocine CoA (Certificate of Analysis) is a formal document that attests to Dezocine's compliance with Dezocine specifications and serves as a tool for batch-level quality control.
Dezocine CoA mostly includes findings from lab analyses of a specific batch. For each Dezocine 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.
Dezocine may be tested according to a variety of international standards, such as European Pharmacopoeia (Dezocine EP), Dezocine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dezocine USP).
