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)
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
0
84
PharmaCompass offers a list of Boldo 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 Boldo manufacturer or Boldo supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Boldo manufacturer or Boldo supplier.
PharmaCompass also assists you with knowing the Boldo API Price utilized in the formulation of products. Boldo API Price is not always fixed or binding as the Boldo Price is obtained through a variety of data sources. The Boldo Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Boldo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boldo, including repackagers and relabelers. The FDA regulates Boldo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boldo 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 Boldo supplier is an individual or a company that provides Boldo active pharmaceutical ingredient (API) or Boldo finished formulations upon request. The Boldo suppliers may include Boldo API manufacturers, exporters, distributors and traders.
Boldo 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 Boldo 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 Boldo GMP manufacturer or Boldo GMP API supplier for your needs.
A Boldo CoA (Certificate of Analysis) is a formal document that attests to Boldo's compliance with Boldo specifications and serves as a tool for batch-level quality control.
Boldo CoA mostly includes findings from lab analyses of a specific batch. For each Boldo 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.
Boldo may be tested according to a variety of international standards, such as European Pharmacopoeia (Boldo EP), Boldo JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Boldo USP).