Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 2BACHEM S.A. Vionnaz CH
02 1FERMION OY Espoo FI
03 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
04 1DIVI'S LABORATORIES LIMITED Hyderabad IN
05 1EGIS Pharmaceuticals PLC Budapest HU
06 1Glochem Industries Limited Hyderabad IN
07 1HETERO DRUGS LIMITED Hyderabad IN
08 1Kraemer & Martin Pharma Handels GmbH Krefeld DE
09 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
10 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
11 1Smruthi Organics Limited Solapur IN
12 1TAPI NL B.V. Amsterdam NL
13 1ZHEJIANG WILD WIND PHARMACEUTICAL CO., LTD. Geshan Town CN
14 2Zhejiang Chiral Medicine Chemicals Co., Ltd. Hangzhou CN
15 2Zhejiang Yongtai Chiral Medicine Technology Co., Ltd. Taizhou City CN
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : R1-CEP 2000-012 - Rev 08
Status : Valid
Issue Date : 2019-12-16
Type : Chemical
Substance Number : 755
With Fermion, start the journey of your innovative API.
Certificate Number : CEP 2011-275 - Rev 02
Status : Valid
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 755
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2001-352 - Rev 08
Status : Valid
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 755
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Certificate Number : R0-CEP 2020-364 - Rev 00
Status : Valid
Issue Date : 2021-06-22
Type : Chemical
Substance Number : 755
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PharmaCompass offers a list of Carbidopa 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 Carbidopa manufacturer or Carbidopa supplier for your needs.
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A RYTARY manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RYTARY, including repackagers and relabelers. The FDA regulates RYTARY manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RYTARY 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 RYTARY supplier is an individual or a company that provides RYTARY active pharmaceutical ingredient (API) or RYTARY finished formulations upon request. The RYTARY suppliers may include RYTARY API manufacturers, exporters, distributors and traders.
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A RYTARY CEP of the European Pharmacopoeia monograph is often referred to as a RYTARY Certificate of Suitability (COS). The purpose of a RYTARY CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of RYTARY EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of RYTARY to their clients by showing that a RYTARY CEP has been issued for it. The manufacturer submits a RYTARY CEP (COS) as part of the market authorization procedure, and it takes on the role of a RYTARY CEP holder for the record. Additionally, the data presented in the RYTARY CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the RYTARY DMF.
A RYTARY CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. RYTARY 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 RYTARY suppliers with CEP (COS) on PharmaCompass.
We have 13 companies offering RYTARY
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