API Suppliers
0
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
EU WC
0
Listed Suppliers
0
0
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
75
PharmaCompass offers a list of Rhein 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 Rhein manufacturer or Rhein supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rhein manufacturer or Rhein supplier.
PharmaCompass also assists you with knowing the Rhein API Price utilized in the formulation of products. Rhein API Price is not always fixed or binding as the Rhein Price is obtained through a variety of data sources. The Rhein Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rhein manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rhein, including repackagers and relabelers. The FDA regulates Rhein manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rhein 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 Rhein supplier is an individual or a company that provides Rhein active pharmaceutical ingredient (API) or Rhein finished formulations upon request. The Rhein suppliers may include Rhein API manufacturers, exporters, distributors and traders.
Rhein 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 Rhein 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 Rhein GMP manufacturer or Rhein GMP API supplier for your needs.
A Rhein CoA (Certificate of Analysis) is a formal document that attests to Rhein's compliance with Rhein specifications and serves as a tool for batch-level quality control.
Rhein CoA mostly includes findings from lab analyses of a specific batch. For each Rhein 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.
Rhein may be tested according to a variety of international standards, such as European Pharmacopoeia (Rhein EP), Rhein JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rhein USP).