Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19103
Submission : 2005-10-28
Status :
Type : IV
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19102
Submission : 2005-10-28
Status :
Type : IV
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 Imports and Exports
Upgrade, download data, analyse, strategize, subscribe with us 
Market Place
ABOUT THIS PAGE
A L-Lactide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Lactide, including repackagers and relabelers. The FDA regulates L-Lactide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Lactide 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 L-Lactide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-Lactide supplier is an individual or a company that provides L-Lactide active pharmaceutical ingredient (API) or L-Lactide finished formulations upon request. The L-Lactide suppliers may include L-Lactide API manufacturers, exporters, distributors and traders.
click here to find a list of L-Lactide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A L-Lactide DMF (Drug Master File) is a document detailing the whole manufacturing process of L-Lactide active pharmaceutical ingredient (API) in detail. Different forms of L-Lactide DMFs exist exist since differing nations have different regulations, such as L-Lactide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A L-Lactide DMF submitted to regulatory agencies in the US is known as a USDMF. L-Lactide USDMF includes data on L-Lactide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The L-Lactide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of L-Lactide suppliers with USDMF on PharmaCompass.
L-Lactide 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 L-Lactide 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 L-Lactide GMP manufacturer or L-Lactide GMP API supplier for your needs.
A L-Lactide CoA (Certificate of Analysis) is a formal document that attests to L-Lactide's compliance with L-Lactide specifications and serves as a tool for batch-level quality control.
L-Lactide CoA mostly includes findings from lab analyses of a specific batch. For each L-Lactide 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.
L-Lactide may be tested according to a variety of international standards, such as European Pharmacopoeia (L-Lactide EP), L-Lactide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (L-Lactide USP).
LOOKING FOR A SUPPLIER?
