X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
Canada
0
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
0
19
PharmaCompass offers a list of Rosuvastatin 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 Rosuvastatin manufacturer or Rosuvastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rosuvastatin manufacturer or Rosuvastatin supplier.
PharmaCompass also assists you with knowing the Rosuvastatin API Price utilized in the formulation of products. Rosuvastatin API Price is not always fixed or binding as the Rosuvastatin Price is obtained through a variety of data sources. The Rosuvastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rosuvastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rosuvastatin, including repackagers and relabelers. The FDA regulates Rosuvastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rosuvastatin 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 Rosuvastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rosuvastatin supplier is an individual or a company that provides Rosuvastatin active pharmaceutical ingredient (API) or Rosuvastatin finished formulations upon request. The Rosuvastatin suppliers may include Rosuvastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Rosuvastatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rosuvastatin DMF (Drug Master File) is a document detailing the whole manufacturing process of Rosuvastatin active pharmaceutical ingredient (API) in detail. Different forms of Rosuvastatin DMFs exist exist since differing nations have different regulations, such as Rosuvastatin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rosuvastatin DMF submitted to regulatory agencies in the US is known as a USDMF. Rosuvastatin USDMF includes data on Rosuvastatin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rosuvastatin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rosuvastatin suppliers with USDMF on PharmaCompass.
Rosuvastatin 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 Rosuvastatin 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 Rosuvastatin GMP manufacturer or Rosuvastatin GMP API supplier for your needs.
A Rosuvastatin CoA (Certificate of Analysis) is a formal document that attests to Rosuvastatin's compliance with Rosuvastatin specifications and serves as a tool for batch-level quality control.
Rosuvastatin CoA mostly includes findings from lab analyses of a specific batch. For each Rosuvastatin 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.
Rosuvastatin may be tested according to a variety of international standards, such as European Pharmacopoeia (Rosuvastatin EP), Rosuvastatin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rosuvastatin USP).
Market Place
