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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Testosterone Enanthate manufacturer or Testosterone Enanthate supplier.
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 Androtardyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Androtardyl, including repackagers and relabelers. The FDA regulates Androtardyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Androtardyl 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 Androtardyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Androtardyl supplier is an individual or a company that provides Androtardyl active pharmaceutical ingredient (API) or Androtardyl finished formulations upon request. The Androtardyl suppliers may include Androtardyl API manufacturers, exporters, distributors and traders.
click here to find a list of Androtardyl 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 Androtardyl Drug Master File in Japan (Androtardyl JDMF) empowers Androtardyl 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 Androtardyl JDMF during the approval evaluation for pharmaceutical products. At the time of Androtardyl 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 Androtardyl suppliers with JDMF on PharmaCompass.
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