X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
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
22
PharmaCompass offers a list of L-Lactide 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-Lactide manufacturer or L-Lactide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Lactide manufacturer or L-Lactide supplier.
PharmaCompass also assists you with knowing the L-Lactide API Price utilized in the formulation of products. L-Lactide API Price is not always fixed or binding as the L-Lactide Price is obtained through a variety of data sources. The L-Lactide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dilactide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dilactide, including repackagers and relabelers. The FDA regulates Dilactide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dilactide 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 Dilactide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dilactide supplier is an individual or a company that provides Dilactide active pharmaceutical ingredient (API) or Dilactide finished formulations upon request. The Dilactide suppliers may include Dilactide API manufacturers, exporters, distributors and traders.
click here to find a list of Dilactide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dilactide DMF (Drug Master File) is a document detailing the whole manufacturing process of Dilactide active pharmaceutical ingredient (API) in detail. Different forms of Dilactide DMFs exist exist since differing nations have different regulations, such as Dilactide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dilactide DMF submitted to regulatory agencies in the US is known as a USDMF. Dilactide USDMF includes data on Dilactide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dilactide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dilactide suppliers with USDMF on PharmaCompass.
Dilactide 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 Dilactide 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 Dilactide GMP manufacturer or Dilactide GMP API supplier for your needs.
A Dilactide CoA (Certificate of Analysis) is a formal document that attests to Dilactide's compliance with Dilactide specifications and serves as a tool for batch-level quality control.
Dilactide CoA mostly includes findings from lab analyses of a specific batch. For each Dilactide 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.
Dilactide may be tested according to a variety of international standards, such as European Pharmacopoeia (Dilactide EP), Dilactide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dilactide USP).
Market Place
