Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 2Evonik
02 1Boehringer Ingelheim GmbH
03 1Diqi Pharmaceutical
01 1POLY(D,L-LACTIDE)
02 1POLY(D,L-LACTIDE) AND ITS COPOLYMERS
03 1RESOMER® R FOR PHARMACEUTICAL APPLICATIONS
04 1RESOMER® RG FOR PHARMACEUTICAL APPLICATIONS
01 1China
02 3Germany
01 3Active
02 1Inactive
01 4Blank
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 : Active
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 : 19103
Submission : 2005-10-28
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12983
Submission : 1998-04-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37673
Submission : 2022-12-08
Status : Active
Type : IV
80
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.
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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 MolPort-001-783-272 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-783-272, including repackagers and relabelers. The FDA regulates MolPort-001-783-272 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-783-272 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MolPort-001-783-272 supplier is an individual or a company that provides MolPort-001-783-272 active pharmaceutical ingredient (API) or MolPort-001-783-272 finished formulations upon request. The MolPort-001-783-272 suppliers may include MolPort-001-783-272 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-783-272 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-783-272 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-783-272 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-783-272 DMFs exist exist since differing nations have different regulations, such as MolPort-001-783-272 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-783-272 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-783-272 USDMF includes data on MolPort-001-783-272's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-783-272 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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