01 1PEPTIDO GmbH
01 1Liothyronine sodium
01 1Germany
Registration Number : 222MF10255
Registrant's Address : Am Kraftwerk 6, D-66450 Bexbach, Germany
Initial Date of Registration : 2010-11-05
Latest Date of Registration : 2010-11-05
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PharmaCompass offers a list of Liothyronine Sodium 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 Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Liothyronine Sodium manufacturer or Liothyronine Sodium supplier.
PharmaCompass also assists you with knowing the Liothyronine Sodium API Price utilized in the formulation of products. Liothyronine Sodium API Price is not always fixed or binding as the Liothyronine Sodium Price is obtained through a variety of data sources. The Liothyronine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Liothyronin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liothyronin, including repackagers and relabelers. The FDA regulates Liothyronin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liothyronin 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 Liothyronin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Liothyronin supplier is an individual or a company that provides Liothyronin active pharmaceutical ingredient (API) or Liothyronin finished formulations upon request. The Liothyronin suppliers may include Liothyronin API manufacturers, exporters, distributors and traders.
click here to find a list of Liothyronin 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 Liothyronin Drug Master File in Japan (Liothyronin JDMF) empowers Liothyronin 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 Liothyronin JDMF during the approval evaluation for pharmaceutical products. At the time of Liothyronin 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 Liothyronin suppliers with JDMF on PharmaCompass.
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