Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
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01 1Bachem AG
02 1CHEMI S. p. A.
03 1Hamari Pharmaceuticals Co., Ltd.
04 1SUN PHARMACEUTICAL INDUSTRIES LTD.
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01 2Octreotide Acetate
02 1Octreotide acetate
03 1Octreotide acetate "CHEMI"
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01 1India
02 1Italy
03 1Japan
04 1Switzerland
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
Registration Number : 306MF10083
Registrant's Address : Hauptstrasse 144,4416 Bubendorf Switzerland
Initial Date of Registration : 2024-07-03
Latest Date of Registration : 2024-07-03
Registration Number : 226MF10055
Registrant's Address : Viale dei Laboratori 54, 20092 Cinisello Balsamo (Milano) ITALY
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2014-03-06
Registration Number : 227MF10055
Registrant's Address : 1-4-29 Shibashima, Higashiyodogawa-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2015-02-18
Latest Date of Registration : 2015-02-18
Registration Number : 226MF10062
Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2014-03-06
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PharmaCompass offers a list of Octreotide 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 Octreotide Acetate manufacturer or Octreotide Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Octreotide Acetate API Price utilized in the formulation of products. Octreotide Acetate API Price is not always fixed or binding as the Octreotide Acetate Price is obtained through a variety of data sources. The Octreotide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Octreotide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Octreotide, including repackagers and relabelers. The FDA regulates Octreotide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Octreotide 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 Octreotide supplier is an individual or a company that provides Octreotide active pharmaceutical ingredient (API) or Octreotide finished formulations upon request. The Octreotide suppliers may include Octreotide API manufacturers, exporters, distributors and traders.
click here to find a list of Octreotide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Octreotide Drug Master File in Japan (Octreotide JDMF) empowers Octreotide 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 Octreotide JDMF during the approval evaluation for pharmaceutical products. At the time of Octreotide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Octreotide suppliers with JDMF on PharmaCompass.
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