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 LIGNOSPAN FORTE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIGNOSPAN FORTE, including repackagers and relabelers. The FDA regulates LIGNOSPAN FORTE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIGNOSPAN FORTE 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 LIGNOSPAN FORTE supplier is an individual or a company that provides LIGNOSPAN FORTE active pharmaceutical ingredient (API) or LIGNOSPAN FORTE finished formulations upon request. The LIGNOSPAN FORTE suppliers may include LIGNOSPAN FORTE 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 LIGNOSPAN FORTE Drug Master File in Japan (LIGNOSPAN FORTE JDMF) empowers LIGNOSPAN FORTE 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 LIGNOSPAN FORTE JDMF during the approval evaluation for pharmaceutical products. At the time of LIGNOSPAN FORTE 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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