01 1S. I. M. S. S. r. l.
01 1Outsiders regulations tetrahydrozoline hydrochloride (production only)
01 1Italy
Tetrahydrozoline Hydrochloride (for manufacturing purposes 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 Tetryzolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetryzolin, including repackagers and relabelers. The FDA regulates Tetryzolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetryzolin 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 Tetryzolin supplier is an individual or a company that provides Tetryzolin active pharmaceutical ingredient (API) or Tetryzolin finished formulations upon request. The Tetryzolin suppliers may include Tetryzolin API manufacturers, exporters, distributors and traders.
click here to find a list of Tetryzolin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Tetryzolin Drug Master File in Japan (Tetryzolin JDMF) empowers Tetryzolin 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 Tetryzolin JDMF during the approval evaluation for pharmaceutical products. At the time of Tetryzolin 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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