Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
01 1Bachem Americas, Inc.
02 1Hamari PFST Co., Ltd.
03 1Polypeptide Laboratories, Inc.
01 1Teriparatide Acetate
02 2Teriparatide acetate
01 1Japan
02 2Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 228MF10213
Registrant's Address : 3132 Kashiwa Street, Torrance, California 90505, USA
Initial Date of Registration : 2016-11-09
Latest Date of Registration : 2016-11-09
Registration Number : 231MF10059
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2019-02-25
Latest Date of Registration : 2023-03-15
Registration Number : 230MF10022
Registrant's Address : 365 Maple Avenue, Torrance, CA 90503, U.S. S. A
Initial Date of Registration : 2018-02-14
Latest Date of Registration : 2018-02-14
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PharmaCompass offers a list of Teriparatide 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 Teriparatide Acetate manufacturer or Teriparatide Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Teriparatide Acetate API Price utilized in the formulation of products. Teriparatide Acetate API Price is not always fixed or binding as the Teriparatide Acetate Price is obtained through a variety of data sources. The Teriparatide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Parathar Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parathar Acetate, including repackagers and relabelers. The FDA regulates Parathar Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parathar Acetate 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 Parathar Acetate supplier is an individual or a company that provides Parathar Acetate active pharmaceutical ingredient (API) or Parathar Acetate finished formulations upon request. The Parathar Acetate suppliers may include Parathar Acetate API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Parathar Acetate Drug Master File in Japan (Parathar Acetate JDMF) empowers Parathar Acetate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Parathar Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Parathar Acetate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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