01 1BCN Peptides S. A.
02 1Polypeptide Laboratories, Inc.
01 1Gonadorelin Diacetate
02 1Gonadorelin acetate
01 1Spain
02 1Switzerland
Registration Number : 305MF10023
Registrant's Address : Poligono industrial Els Vinyets-Els Fogars. Sector II 08777-Sant Quinti de Mediona, B...
Initial Date of Registration : 2023-02-08
Latest Date of Registration : 2023-02-08
Registration Number : 219MF10020
Registrant's Address : 365 Maple Avenue, Torrance, CA 90503, USA
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2007-01-22
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PharmaCompass offers a list of Gonadorelin Acetate 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 Gonadorelin Acetate manufacturer or Gonadorelin Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gonadorelin Acetate manufacturer or Gonadorelin Acetate supplier.
PharmaCompass also assists you with knowing the Gonadorelin Acetate API Price utilized in the formulation of products. Gonadorelin Acetate API Price is not always fixed or binding as the Gonadorelin Acetate Price is obtained through a variety of data sources. The Gonadorelin Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutrelef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutrelef, including repackagers and relabelers. The FDA regulates Lutrelef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutrelef 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 Lutrelef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutrelef supplier is an individual or a company that provides Lutrelef active pharmaceutical ingredient (API) or Lutrelef finished formulations upon request. The Lutrelef suppliers may include Lutrelef API manufacturers, exporters, distributors and traders.
click here to find a list of Lutrelef 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 Lutrelef Drug Master File in Japan (Lutrelef JDMF) empowers Lutrelef 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 Lutrelef JDMF during the approval evaluation for pharmaceutical products. At the time of Lutrelef 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 Lutrelef suppliers with JDMF on PharmaCompass.
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