X
API Suppliers
0
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
0
USA (Orange Book)
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
95
PharmaCompass offers a list of Desirudin 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 Desirudin manufacturer or Desirudin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desirudin manufacturer or Desirudin supplier.
PharmaCompass also assists you with knowing the Desirudin API Price utilized in the formulation of products. Desirudin API Price is not always fixed or binding as the Desirudin Price is obtained through a variety of data sources. The Desirudin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Desirudin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desirudin, including repackagers and relabelers. The FDA regulates Desirudin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desirudin 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 Desirudin supplier is an individual or a company that provides Desirudin active pharmaceutical ingredient (API) or Desirudin finished formulations upon request. The Desirudin suppliers may include Desirudin API manufacturers, exporters, distributors and traders.
Desirudin 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 Desirudin 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 Desirudin GMP manufacturer or Desirudin GMP API supplier for your needs.
A Desirudin CoA (Certificate of Analysis) is a formal document that attests to Desirudin's compliance with Desirudin specifications and serves as a tool for batch-level quality control.
Desirudin CoA mostly includes findings from lab analyses of a specific batch. For each Desirudin 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.
Desirudin may be tested according to a variety of international standards, such as European Pharmacopoeia (Desirudin EP), Desirudin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Desirudin USP).
Market Place
