ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
01 1ChemWerth Inc
02 2Bachem AG
03 1GLAND PHARMA LIMITED
04 1Johnson & Johnson Innovative Medicine
05 1Pisgah Labs
06 1Reliable Biopharmaceutical Corporation
07 1Solara Active Pharma Sciences
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-24
Pay. Date : 2013-06-13
DMF Number : 20500
Submission : 2007-04-30
Status :
Type : II
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-16
Pay. Date : 2014-10-14
DMF Number : 20234
Submission : 2007-01-29
Status :
Type : II
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38855
Submission : 2023-09-19
Status :
Type : II
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PharmaCompass offers a list of Etomidate 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 Etomidate manufacturer or Etomidate supplier for your needs.
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A MolPort-000-917-569 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-917-569, including repackagers and relabelers. The FDA regulates MolPort-000-917-569 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-917-569 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-000-917-569 supplier is an individual or a company that provides MolPort-000-917-569 active pharmaceutical ingredient (API) or MolPort-000-917-569 finished formulations upon request. The MolPort-000-917-569 suppliers may include MolPort-000-917-569 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-000-917-569 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-000-917-569 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-000-917-569 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-000-917-569 DMFs exist exist since differing nations have different regulations, such as MolPort-000-917-569 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-000-917-569 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-000-917-569 USDMF includes data on MolPort-000-917-569's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-000-917-569 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MolPort-000-917-569 suppliers with USDMF on PharmaCompass.
We have 7 companies offering MolPort-000-917-569
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