Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem AG Bubendorf CH
02 2ASPEN OSS B.V. Oss NL
03 2BCN PEPTIDES S.A. St Quinti De Mediona ES
04 1CHEMI S.P.A. Patrica IT
05 1HYBIO PHARMACEUTICAL CO., LTD. Shenzhen CN
06 1MALLINCKRODT, INC. Hazelwood US
07 1PIRAMAL PHARMA LIMITED Navi Mumbai IN
08 1POLYPEPTIDE LABORATORIES (SWEDEN) AB Limhamn SE
09 1PolyPeptide Laboratories Inc. Torrance US
10 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
11 1Takeda Pharmaceutical Company, Limited Osaka JP
12 1ZHEJIANG PEPTITES BIOTECH CO., LTD. Sanjie Town CN
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : R1-CEP 2001-454 - Rev 01
Status : Valid
Issue Date : 2009-02-18
Type : Chemical
Substance Number : 1442
Aspen API. More than just an API™
Certificate Number : R0-CEP 2021-472 - Rev 00
Status : Valid
Issue Date : 2022-02-28
Type : Chemical
Substance Number : 1442
Aspen API. More than just an API™
Certificate Number : R1-CEP 2016-199 - Rev 00
Status : Valid
Issue Date : 2022-08-26
Type : Chemical
Substance Number : 1442
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PharmaCompass offers a list of Leuprolide Acetate 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 Leuprolide Acetate manufacturer or Leuprolide Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Leuprolide Acetate API Price utilized in the formulation of products. Leuprolide Acetate API Price is not always fixed or binding as the Leuprolide Acetate Price is obtained through a variety of data sources. The Leuprolide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutrate (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutrate (TN), including repackagers and relabelers. The FDA regulates Lutrate (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutrate (TN) 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 Lutrate (TN) supplier is an individual or a company that provides Lutrate (TN) active pharmaceutical ingredient (API) or Lutrate (TN) finished formulations upon request. The Lutrate (TN) suppliers may include Lutrate (TN) API manufacturers, exporters, distributors and traders.
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A Lutrate (TN) CEP of the European Pharmacopoeia monograph is often referred to as a Lutrate (TN) Certificate of Suitability (COS). The purpose of a Lutrate (TN) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lutrate (TN) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lutrate (TN) to their clients by showing that a Lutrate (TN) CEP has been issued for it. The manufacturer submits a Lutrate (TN) CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lutrate (TN) CEP holder for the record. Additionally, the data presented in the Lutrate (TN) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lutrate (TN) DMF.
A Lutrate (TN) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lutrate (TN) CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Lutrate (TN) suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Lutrate (TN)
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