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
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PharmaCompass offers a list of Testosterone Enanthate 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 Testosterone Enanthate manufacturer or Testosterone Enanthate supplier for your needs.
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PharmaCompass also assists you with knowing the Testosterone Enanthate API Price utilized in the formulation of products. Testosterone Enanthate API Price is not always fixed or binding as the Testosterone Enanthate Price is obtained through a variety of data sources. The Testosterone Enanthate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Testosteron-Depot Eifelfango manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Testosteron-Depot Eifelfango, including repackagers and relabelers. The FDA regulates Testosteron-Depot Eifelfango manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Testosteron-Depot Eifelfango 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 Testosteron-Depot Eifelfango supplier is an individual or a company that provides Testosteron-Depot Eifelfango active pharmaceutical ingredient (API) or Testosteron-Depot Eifelfango finished formulations upon request. The Testosteron-Depot Eifelfango suppliers may include Testosteron-Depot Eifelfango API manufacturers, exporters, distributors and traders.
click here to find a list of Testosteron-Depot Eifelfango 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 Testosteron-Depot Eifelfango Drug Master File in Japan (Testosteron-Depot Eifelfango JDMF) empowers Testosteron-Depot Eifelfango 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 Testosteron-Depot Eifelfango JDMF during the approval evaluation for pharmaceutical products. At the time of Testosteron-Depot Eifelfango 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 Testosteron-Depot Eifelfango suppliers with JDMF on PharmaCompass.
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