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
A Tetrahydrozoline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetrahydrozoline Hydrochloride, including repackagers and relabelers. The FDA regulates Tetrahydrozoline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetrahydrozoline Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tetrahydrozoline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetrahydrozoline Hydrochloride supplier is an individual or a company that provides Tetrahydrozoline Hydrochloride active pharmaceutical ingredient (API) or Tetrahydrozoline Hydrochloride finished formulations upon request. The Tetrahydrozoline Hydrochloride suppliers may include Tetrahydrozoline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tetrahydrozoline Hydrochloride 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 Tetrahydrozoline Hydrochloride Drug Master File in Japan (Tetrahydrozoline Hydrochloride JDMF) empowers Tetrahydrozoline Hydrochloride 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 Tetrahydrozoline Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Tetrahydrozoline Hydrochloride 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 Tetrahydrozoline Hydrochloride suppliers with JDMF on PharmaCompass.
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