01 1Cambrex Profarmaco Milano S. r. l.
02 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Adrenalin
02 1Epinephrine
01 1Taiwan
02 1U.S.A
Registration Number : 226MF10196
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2020-04-22
Registration Number : 230MF10047
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2018-03-27
Latest Date of Registration : 2018-03-27
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PharmaCompass offers a list of Epinephrine 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 Epinephrine manufacturer or Epinephrine supplier for your needs.
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PharmaCompass also assists you with knowing the Epinephrine API Price utilized in the formulation of products. Epinephrine API Price is not always fixed or binding as the Epinephrine Price is obtained through a variety of data sources. The Epinephrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A nchembio747-comp9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nchembio747-comp9, including repackagers and relabelers. The FDA regulates nchembio747-comp9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nchembio747-comp9 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 nchembio747-comp9 supplier is an individual or a company that provides nchembio747-comp9 active pharmaceutical ingredient (API) or nchembio747-comp9 finished formulations upon request. The nchembio747-comp9 suppliers may include nchembio747-comp9 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 nchembio747-comp9 Drug Master File in Japan (nchembio747-comp9 JDMF) empowers nchembio747-comp9 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 nchembio747-comp9 JDMF during the approval evaluation for pharmaceutical products. At the time of nchembio747-comp9 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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