01 1STEROID S. p. A.
01 1Testosterone Enanthate
01 1Italy
Registration Number : 304MF10082
Registrant's Address : Viale Spagna, 156 Cologno Monzese (MI) - ITALY
Initial Date of Registration : 2022-06-01
Latest Date of Registration : 2022-06-01
A Testosterone Enanthate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Testosterone Enanthate, including repackagers and relabelers. The FDA regulates Testosterone Enanthate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Testosterone Enanthate 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 Testosterone Enanthate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Testosterone Enanthate supplier is an individual or a company that provides Testosterone Enanthate active pharmaceutical ingredient (API) or Testosterone Enanthate finished formulations upon request. The Testosterone Enanthate suppliers may include Testosterone Enanthate API manufacturers, exporters, distributors and traders.
click here to find a list of Testosterone Enanthate 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 Testosterone Enanthate Drug Master File in Japan (Testosterone Enanthate JDMF) empowers Testosterone Enanthate 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 Testosterone Enanthate JDMF during the approval evaluation for pharmaceutical products. At the time of Testosterone Enanthate 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 Testosterone Enanthate suppliers with JDMF on PharmaCompass.
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