Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
02 1ALP Pharm
03 1AmbioPharm
04 1Apicore LLC
05 1Asymchem Laboratories
06 1Aurisco Pharmaceutical
07 1Beijing QL Biopharmaceutical
08 1Biocon
09 1Chengdu Shengnuo Biopharm
10 1Chinese Peptide Company
11 2Fujian Genohope Biotech
12 1Hangzhou Go Top Peptide Biotech Co.,Ltd
13 1Hangzhou Zhongmei Huadong Pharmaceutical
14 1Huisheng Biopharmaceutical
15 1Hybio Pharmaceutical
16 1Jiangsu Sinopep Allsino Biopharmaceutical
17 1MSN Laboratories
18 2PolyPeptide Group
19 1Shenzhen JYMed Technology
20 1Sun Pharmaceutical Industries Limited
21 1Suzhou Ryway Biotech
22 1Suzhou Tianma Pharma Group Co Ltd
23 1Xiamen SINOPEG Biotech
24 1Zhejiang Peptites Biotech Co.,Ltd
25 1Zydus Lifesciences
26 9Blank
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
GDUFA
DMF Review : Complete
Rev. Date : 2024-04-30
Pay. Date : 2023-03-02
DMF Number : 37594
Submission : 2023-03-16
Status :
Type : II
59
PharmaCompass offers a list of Semaglutide 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 Semaglutide manufacturer or Semaglutide supplier for your needs.
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A Semaglutide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Semaglutide, including repackagers and relabelers. The FDA regulates Semaglutide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Semaglutide 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 Semaglutide supplier is an individual or a company that provides Semaglutide active pharmaceutical ingredient (API) or Semaglutide finished formulations upon request. The Semaglutide suppliers may include Semaglutide API manufacturers, exporters, distributors and traders.
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A Semaglutide DMF (Drug Master File) is a document detailing the whole manufacturing process of Semaglutide active pharmaceutical ingredient (API) in detail. Different forms of Semaglutide DMFs exist exist since differing nations have different regulations, such as Semaglutide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Semaglutide DMF submitted to regulatory agencies in the US is known as a USDMF. Semaglutide USDMF includes data on Semaglutide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Semaglutide USDMF is kept confidential to protect the manufacturer’s intellectual property.
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