01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Epinephrine Hydrogentrate
01 1Taiwan
Registration Number : 303MF10034
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2021-02-16
Latest Date of Registration : 2021-02-16
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PharmaCompass offers a list of Epinephrine Bitartrate 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 Bitartrate manufacturer or Epinephrine Bitartrate supplier for your needs.
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PharmaCompass also assists you with knowing the Epinephrine Bitartrate API Price utilized in the formulation of products. Epinephrine Bitartrate API Price is not always fixed or binding as the Epinephrine Bitartrate Price is obtained through a variety of data sources. The Epinephrine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Adrenaline acid tartrate, l- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adrenaline acid tartrate, l-, including repackagers and relabelers. The FDA regulates Adrenaline acid tartrate, l- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adrenaline acid tartrate, l- 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 Adrenaline acid tartrate, l- supplier is an individual or a company that provides Adrenaline acid tartrate, l- active pharmaceutical ingredient (API) or Adrenaline acid tartrate, l- finished formulations upon request. The Adrenaline acid tartrate, l- suppliers may include Adrenaline acid tartrate, l- 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 Adrenaline acid tartrate, l- Drug Master File in Japan (Adrenaline acid tartrate, l- JDMF) empowers Adrenaline acid tartrate, l- 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 Adrenaline acid tartrate, l- JDMF during the approval evaluation for pharmaceutical products. At the time of Adrenaline acid tartrate, l- 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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