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
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
15
PharmaCompass offers a list of L-Tartaric Acid 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 L-Tartaric Acid manufacturer or L-Tartaric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Tartaric Acid manufacturer or L-Tartaric Acid supplier.
PharmaCompass also assists you with knowing the L-Tartaric Acid API Price utilized in the formulation of products. L-Tartaric Acid API Price is not always fixed or binding as the L-Tartaric Acid Price is obtained through a variety of data sources. The L-Tartaric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 000189E3-11D0-4B0A-8C7B-31E02A48A51F manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 000189E3-11D0-4B0A-8C7B-31E02A48A51F, including repackagers and relabelers. The FDA regulates 000189E3-11D0-4B0A-8C7B-31E02A48A51F manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 000189E3-11D0-4B0A-8C7B-31E02A48A51F 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 000189E3-11D0-4B0A-8C7B-31E02A48A51F manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 000189E3-11D0-4B0A-8C7B-31E02A48A51F supplier is an individual or a company that provides 000189E3-11D0-4B0A-8C7B-31E02A48A51F active pharmaceutical ingredient (API) or 000189E3-11D0-4B0A-8C7B-31E02A48A51F finished formulations upon request. The 000189E3-11D0-4B0A-8C7B-31E02A48A51F suppliers may include 000189E3-11D0-4B0A-8C7B-31E02A48A51F API manufacturers, exporters, distributors and traders.
click here to find a list of 000189E3-11D0-4B0A-8C7B-31E02A48A51F suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 000189E3-11D0-4B0A-8C7B-31E02A48A51F DMF (Drug Master File) is a document detailing the whole manufacturing process of 000189E3-11D0-4B0A-8C7B-31E02A48A51F active pharmaceutical ingredient (API) in detail. Different forms of 000189E3-11D0-4B0A-8C7B-31E02A48A51F DMFs exist exist since differing nations have different regulations, such as 000189E3-11D0-4B0A-8C7B-31E02A48A51F USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 000189E3-11D0-4B0A-8C7B-31E02A48A51F DMF submitted to regulatory agencies in the US is known as a USDMF. 000189E3-11D0-4B0A-8C7B-31E02A48A51F USDMF includes data on 000189E3-11D0-4B0A-8C7B-31E02A48A51F's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 000189E3-11D0-4B0A-8C7B-31E02A48A51F USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 000189E3-11D0-4B0A-8C7B-31E02A48A51F suppliers with USDMF on PharmaCompass.
000189E3-11D0-4B0A-8C7B-31E02A48A51F 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 000189E3-11D0-4B0A-8C7B-31E02A48A51F 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 000189E3-11D0-4B0A-8C7B-31E02A48A51F GMP manufacturer or 000189E3-11D0-4B0A-8C7B-31E02A48A51F GMP API supplier for your needs.
A 000189E3-11D0-4B0A-8C7B-31E02A48A51F CoA (Certificate of Analysis) is a formal document that attests to 000189E3-11D0-4B0A-8C7B-31E02A48A51F's compliance with 000189E3-11D0-4B0A-8C7B-31E02A48A51F specifications and serves as a tool for batch-level quality control.
000189E3-11D0-4B0A-8C7B-31E02A48A51F CoA mostly includes findings from lab analyses of a specific batch. For each 000189E3-11D0-4B0A-8C7B-31E02A48A51F 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.
000189E3-11D0-4B0A-8C7B-31E02A48A51F may be tested according to a variety of international standards, such as European Pharmacopoeia (000189E3-11D0-4B0A-8C7B-31E02A48A51F EP), 000189E3-11D0-4B0A-8C7B-31E02A48A51F JP (Japanese Pharmacopeia) and the US Pharmacopoeia (000189E3-11D0-4B0A-8C7B-31E02A48A51F USP).