Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
ABOUT THIS PAGE
26
PharmaCompass offers a list of Di-P-Toluoyl-D-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 Di-P-Toluoyl-D-Tartaric Acid manufacturer or Di-P-Toluoyl-D-Tartaric Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Di-P-Toluoyl-D-Tartaric Acid manufacturer or Di-P-Toluoyl-D-Tartaric Acid supplier.
PharmaCompass also assists you with knowing the Di-P-Toluoyl-D-Tartaric Acid API Price utilized in the formulation of products. Di-P-Toluoyl-D-Tartaric Acid API Price is not always fixed or binding as the Di-P-Toluoyl-D-Tartaric Acid Price is obtained through a variety of data sources. The Di-P-Toluoyl-D-Tartaric Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (+)-dtta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-dtta, including repackagers and relabelers. The FDA regulates (+)-dtta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-dtta 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 (+)-dtta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-dtta supplier is an individual or a company that provides (+)-dtta active pharmaceutical ingredient (API) or (+)-dtta finished formulations upon request. The (+)-dtta suppliers may include (+)-dtta API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-dtta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+)-dtta DMF (Drug Master File) is a document detailing the whole manufacturing process of (+)-dtta active pharmaceutical ingredient (API) in detail. Different forms of (+)-dtta DMFs exist exist since differing nations have different regulations, such as (+)-dtta USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A (+)-dtta DMF submitted to regulatory agencies in the US is known as a USDMF. (+)-dtta USDMF includes data on (+)-dtta's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The (+)-dtta USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of (+)-dtta suppliers with USDMF on PharmaCompass.
(+)-dtta 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 (+)-dtta 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 (+)-dtta GMP manufacturer or (+)-dtta GMP API supplier for your needs.
A (+)-dtta CoA (Certificate of Analysis) is a formal document that attests to (+)-dtta's compliance with (+)-dtta specifications and serves as a tool for batch-level quality control.
(+)-dtta CoA mostly includes findings from lab analyses of a specific batch. For each (+)-dtta 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.
(+)-dtta may be tested according to a variety of international standards, such as European Pharmacopoeia ((+)-dtta EP), (+)-dtta JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((+)-dtta USP).
