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API SUPPLIERS
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ABOUT THIS PAGE
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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 Resomer R208 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resomer R208, including repackagers and relabelers. The FDA regulates Resomer R208 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resomer R208 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 Resomer R208 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Resomer R208 supplier is an individual or a company that provides Resomer R208 active pharmaceutical ingredient (API) or Resomer R208 finished formulations upon request. The Resomer R208 suppliers may include Resomer R208 API manufacturers, exporters, distributors and traders.
click here to find a list of Resomer R208 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Resomer R208 DMF (Drug Master File) is a document detailing the whole manufacturing process of Resomer R208 active pharmaceutical ingredient (API) in detail. Different forms of Resomer R208 DMFs exist exist since differing nations have different regulations, such as Resomer R208 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Resomer R208 DMF submitted to regulatory agencies in the US is known as a USDMF. Resomer R208 USDMF includes data on Resomer R208's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Resomer R208 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Resomer R208 suppliers with USDMF on PharmaCompass.
Resomer R208 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 Resomer R208 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 Resomer R208 GMP manufacturer or Resomer R208 GMP API supplier for your needs.
A Resomer R208 CoA (Certificate of Analysis) is a formal document that attests to Resomer R208's compliance with Resomer R208 specifications and serves as a tool for batch-level quality control.
Resomer R208 CoA mostly includes findings from lab analyses of a specific batch. For each Resomer R208 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.
Resomer R208 may be tested according to a variety of international standards, such as European Pharmacopoeia (Resomer R208 EP), Resomer R208 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Resomer R208 USP).
