01 1S. I. M. S. S. r. l.
01 1Outsiders regulations tetrahydrozoline hydrochloride (production only)
01 1Italy
Tetrahydrozoline hydrochloride (for manufacturing only)
Registration Number : 218MF10080
Registrant's Address : 50066 Reggello (Firenze) Italy
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-03-23
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PharmaCompass offers a list of Tetrahydrozoline 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 Tetrahydrozoline manufacturer or Tetrahydrozoline supplier for your needs.
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PharmaCompass also assists you with knowing the Tetrahydrozoline API Price utilized in the formulation of products. Tetrahydrozoline API Price is not always fixed or binding as the Tetrahydrozoline Price is obtained through a variety of data sources. The Tetrahydrozoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tyzine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tyzine, including repackagers and relabelers. The FDA regulates Tyzine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tyzine 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 Tyzine supplier is an individual or a company that provides Tyzine active pharmaceutical ingredient (API) or Tyzine finished formulations upon request. The Tyzine suppliers may include Tyzine 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 Tyzine Drug Master File in Japan (Tyzine JDMF) empowers Tyzine 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 Tyzine JDMF during the approval evaluation for pharmaceutical products. At the time of Tyzine 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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