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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetrahydrozoline manufacturer or Tetrahydrozoline supplier.
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 Collyrium Fresh manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Collyrium Fresh, including repackagers and relabelers. The FDA regulates Collyrium Fresh manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Collyrium Fresh 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 Collyrium Fresh supplier is an individual or a company that provides Collyrium Fresh active pharmaceutical ingredient (API) or Collyrium Fresh finished formulations upon request. The Collyrium Fresh suppliers may include Collyrium Fresh API manufacturers, exporters, distributors and traders.
click here to find a list of Collyrium Fresh 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 Collyrium Fresh Drug Master File in Japan (Collyrium Fresh JDMF) empowers Collyrium Fresh 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 Collyrium Fresh JDMF during the approval evaluation for pharmaceutical products. At the time of Collyrium Fresh JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Collyrium Fresh suppliers with JDMF on PharmaCompass.
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