Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
02 1Cambrex Profarmaco Milano S. r. l.
01 1Adrenalin
02 1Epinephrine
01 1Germany
02 1U.S.A
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
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
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
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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, and more, enabling you to easily find the right Epinephrine manufacturer or Epinephrine supplier for your needs.
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A Adrenan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adrenan, including repackagers and relabelers. The FDA regulates Adrenan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adrenan API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Adrenan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Adrenan supplier is an individual or a company that provides Adrenan active pharmaceutical ingredient (API) or Adrenan finished formulations upon request. The Adrenan suppliers may include Adrenan API manufacturers, exporters, distributors and traders.
click here to find a list of Adrenan suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Adrenan Drug Master File in Japan (Adrenan JDMF) empowers Adrenan 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 Adrenan JDMF during the approval evaluation for pharmaceutical products. At the time of Adrenan 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 Adrenan suppliers with JDMF on PharmaCompass.
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