API Suppliers
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
18
PharmaCompass offers a list of Apigenin 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 Apigenin manufacturer or Apigenin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Apigenin manufacturer or Apigenin supplier.
PharmaCompass also assists you with knowing the Apigenin API Price utilized in the formulation of products. Apigenin API Price is not always fixed or binding as the Apigenin Price is obtained through a variety of data sources. The Apigenin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chamomile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chamomile, including repackagers and relabelers. The FDA regulates Chamomile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chamomile 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 Chamomile manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chamomile supplier is an individual or a company that provides Chamomile active pharmaceutical ingredient (API) or Chamomile finished formulations upon request. The Chamomile suppliers may include Chamomile API manufacturers, exporters, distributors and traders.
click here to find a list of Chamomile suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Chamomile Drug Master File in Korea (Chamomile KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Chamomile. The MFDS reviews the Chamomile KDMF as part of the drug registration process and uses the information provided in the Chamomile KDMF to evaluate the safety and efficacy of the drug.
After submitting a Chamomile KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Chamomile API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Chamomile suppliers with KDMF on PharmaCompass.
Chamomile 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 Chamomile 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 Chamomile GMP manufacturer or Chamomile GMP API supplier for your needs.
A Chamomile CoA (Certificate of Analysis) is a formal document that attests to Chamomile's compliance with Chamomile specifications and serves as a tool for batch-level quality control.
Chamomile CoA mostly includes findings from lab analyses of a specific batch. For each Chamomile 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.
Chamomile may be tested according to a variety of international standards, such as European Pharmacopoeia (Chamomile EP), Chamomile JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chamomile USP).