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