01 1Siegfried Evionnaz SA
01 1Tetracaine hydrochloride Tetracaine Hydrochloride
01 1Switzerland
Registration Number : 220MF10198
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2008-09-09
Latest Date of Registration : 2024-06-27
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PharmaCompass offers a list of Tetracaine Hydrochloride 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 Tetracaine Hydrochloride manufacturer or Tetracaine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Tetracaine Hydrochloride API Price utilized in the formulation of products. Tetracaine Hydrochloride API Price is not always fixed or binding as the Tetracaine Hydrochloride Price is obtained through a variety of data sources. The Tetracaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Anacel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anacel, including repackagers and relabelers. The FDA regulates Anacel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anacel 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 Anacel supplier is an individual or a company that provides Anacel active pharmaceutical ingredient (API) or Anacel finished formulations upon request. The Anacel suppliers may include Anacel 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 Anacel Drug Master File in Japan (Anacel JDMF) empowers Anacel 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 Anacel JDMF during the approval evaluation for pharmaceutical products. At the time of Anacel 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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