Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG
02 1Alembic Pharmaceuticals Limited
03 1Amphastar Pharmaceuticals
04 1Auro Peptides Limited
05 1Chengdu Shengnuo Biopharm
06 2Hybio Pharmaceutical
07 1MSN Laboratories
08 1ScinoPharm Taiwan Ltd
09 1Shenzhen JYMed Technology
10 1Sun Pharmaceutical Industries Limited
11 1Blank
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 : 8509
Submission : 1990-04-04
Status :
Type : II
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PharmaCompass offers a list of Teriparatide 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 Teriparatide manufacturer or Teriparatide supplier for your needs.
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PharmaCompass also assists you with knowing the Teriparatide API Price utilized in the formulation of products. Teriparatide API Price is not always fixed or binding as the Teriparatide Price is obtained through a variety of data sources. The Teriparatide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hs-2025 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hs-2025, including repackagers and relabelers. The FDA regulates Hs-2025 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hs-2025 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 Hs-2025 supplier is an individual or a company that provides Hs-2025 active pharmaceutical ingredient (API) or Hs-2025 finished formulations upon request. The Hs-2025 suppliers may include Hs-2025 API manufacturers, exporters, distributors and traders.
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A Hs-2025 DMF (Drug Master File) is a document detailing the whole manufacturing process of Hs-2025 active pharmaceutical ingredient (API) in detail. Different forms of Hs-2025 DMFs exist exist since differing nations have different regulations, such as Hs-2025 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hs-2025 DMF submitted to regulatory agencies in the US is known as a USDMF. Hs-2025 USDMF includes data on Hs-2025's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hs-2025 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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